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CAS No. : | 69226-51-3 | MDL No. : | MFCD01683146 |
Formula : | C2H4Cl3NO3S | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | N/A |
M.W : | 228.48 g/mol | Pubchem ID : | - |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P280-P301+P312-P302+P352-P305+P351+P338 | UN#: | |
Hazard Statements: | H302-H315-H319-H335 | Packing Group: | |
GHS Pictogram: |
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* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
52% | With sulphamoyl chloride In N,N-dimethyl acetamide at 20℃; for 24h; | |
10% | With sulphamoyl chloride; potassium carbonate In toluene at 20℃; for 96h; | |
With formic acid; isocyanate de chlorosulfonyle In dimethyl amine; acetonitrile at 0 - 20℃; for 16.1667h; |
With formic acid; isocyanate de chlorosulfonyle In N,N-dimethyl acetamide; acetonitrile at 20℃; Cooling with ice; | ||
With sulphamoyl chloride In N,N-dimethyl acetamide at 0 - 20℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
95% | Stage #1: styrene; 2,2,2-trichloroethyl sulfamate With tetra(trifluoroacetamidato)dirhodium(II); magnesium oxide In benzene at 0℃; Stage #2: With [bis(acetoxy)iodo]benzene In benzene at 0 - 25℃; for 8h; Further stages.; | |
91% | With bis{rhodium[3,3'-(1,3-phenylene)bis(2,2-dimethylpropanoic acid)]; [bis(acetoxy)iodo]benzene; water at 25℃; for 24h; | |
89% | With tetrakis(μ-trifluoroacetamidato)dirhodium(II); [bis(acetoxy)iodo]benzene; magnesium oxide In benzene at 0 - 25℃; for 8h; |
87% | With [bis(acetoxy)iodo]benzene; rhodium perfluorobutyramide; magnesium oxide In benzene at 5 - 20℃; for 10h; | |
69% | With copper(l) iodide; iodosylbenzene In acetonitrile at 20℃; for 18h; Molecular sieve; Inert atmosphere; | |
48% | With [bis(acetoxy)iodo]benzene; C32H44ClN4O4Rh2*3CH2Cl2 at 20℃; for 3h; Inert atmosphere; | |
25% | With [bis(acetoxy)iodo]benzene; 4 A molecular sieve In acetonitrile at 50℃; | |
With [bis(acetoxy)iodo]benzene; magnesium oxide In chlorobenzene at -10 - 23℃; for 8h; | ||
With bis{rhodium[3,3'-(1,3-phenylene)bis(2,2-dimethylpropanoic acid)]; [bis(acetoxy)iodo]benzene In water at 20℃; for 12h; | 1 preparation2,2,2-trichloroethyl (2-hydroxy-2-phenylethyl)-AminoSulfonate Add Rh2(esp)2 (1.1mg, 1.5mol%) to a 3ml vial,TcesNH2 (0.1 mmol,1.0equiv),Iodobenzene diacetate(80.5 mg, 0.2 mmol, 2 equiv) and 1 ml water and styrene 1.5 eq),The reaction was stirred at room temperature for 12 h.Then raise the temperature to 40 ° C,Adjust the pH to 4,Continue stirring for 36h,Add 5 ml of water to the system and extract with CH2Cl2 (3*10 ml).The organic phase is dried over anhydrous sodium sulfate.filter,The mixture was steamed under reduced pressure, and the residue was purified by silica gel column chromatography.The eluate eluted from a petroleum ether/ethyl acetate gradient of 80:1 to 5:1.Collect the target product,The yield of the two-step separation was 91%. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
88% | Stage #1: 4-vinylbenzyl chloride; 2,2,2-trichloroethyl sulfamate With tetra(trifluoroacetamidato)dirhodium(II); magnesium oxide In benzene at 0℃; Stage #2: With [bis(acetoxy)iodo]benzene In benzene at 0 - 25℃; for 8h; Further stages.; | |
60% | With copper(l) iodide; iodosylbenzene In acetonitrile at 20℃; for 18h; Molecular sieve; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
91% | Stage #1: 1-ethenyl-4-methylbenzene; 2,2,2-trichloroethyl sulfamate With tetra(trifluoroacetamidato)dirhodium(II); magnesium oxide In benzene at 0℃; Stage #2: With [bis(acetoxy)iodo]benzene In benzene at 0 - 25℃; for 8h; Further stages.; | |
58% | With [bis(acetoxy)iodo]benzene; rhodium perfluorobutyramide; magnesium oxide In benzene at 5 - 20℃; for 10h; | |
41% | With copper(l) iodide; iodosylbenzene In acetonitrile at 20℃; for 18h; Molecular sieve; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
82% | With [bis(acetoxy)iodo]benzene; magnesium oxide In chlorobenzene at -10 - 23℃; for 8h; | |
82% | Stage #1: cis-Cyclooctene; 2,2,2-trichloroethyl sulfamate With tetra(trifluoroacetamidato)dirhodium(II); magnesium oxide In benzene at 0℃; Stage #2: With [bis(acetoxy)iodo]benzene In benzene at 0 - 25℃; for 8h; Further stages.; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
80% | With bis{rhodium[3,3'-(1,3-phenylene)bis(2,2-dimethylpropanoic acid)]; [bis(acetoxy)iodo]benzene; acetic acid In benzene at 20℃; for 16h; | |
80% | With bis{rhodium[3,3'-(1,3-phenylene)bis(2,2-dimethylpropanoic acid)]; [bis(acetoxy)iodo]benzene; acetic acid In benzene at 25℃; for 48h; | |
71% | With [bis(acetoxy)iodo]benzene; magnesium oxide In chlorobenzene at -10 - 23℃; for 8h; |
71% | Stage #1: 4-nitrostyrene; 2,2,2-trichloroethyl sulfamate With tetra(trifluoroacetamidato)dirhodium(II); magnesium oxide In benzene at 0℃; Stage #2: With [bis(acetoxy)iodo]benzene In benzene at 0 - 25℃; for 8h; Further stages.; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
72% | Stage #1: 2-Methyl-1-pentene; 2,2,2-trichloroethyl sulfamate With tetra(trifluoroacetamidato)dirhodium(II); magnesium oxide In benzene at 0℃; Stage #2: With [bis(acetoxy)iodo]benzene In benzene at 0 - 25℃; for 8h; Further stages.; | |
61% | With 1,3-bis(2,6-diisopropylphenylimidazol)-2-ylidene copper(I) dibenzoylmethanate; iodosylbenzene In chlorobenzene at 25℃; Inert atmosphere; Molecular sieve; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
95% | With tetrakis(μ-trifluoroacetamidato)dirhodium(II); [bis(acetoxy)iodo]benzene; magnesium oxide In benzene at 0 - 25℃; for 8h; | |
85% | With [bis(acetoxy)iodo]benzene; magnesium oxide In chlorobenzene at -10 - 23℃; for 8h; | |
85% | Stage #1: 1-propenylbenzene; 2,2,2-trichloroethyl sulfamate With tetra(trifluoroacetamidato)dirhodium(II); magnesium oxide In benzene at 0℃; Stage #2: With PbI(OAc)2 In benzene at 0 - 25℃; for 8h; Further stages.; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
72% | Stage #1: citronellyl-acetate; 2,2,2-trichloroethyl sulfamate With tetra(trifluoroacetamidato)dirhodium(II); magnesium oxide In benzene at 0℃; Stage #2: With [bis(acetoxy)iodo]benzene In benzene at 0 - 25℃; for 8h; Further stages.; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
72% | Stage #1: (Z)-2-decene; 2,2,2-trichloroethyl sulfamate With tetra(trifluoroacetamidato)dirhodium(II); magnesium oxide In benzene at 0℃; Stage #2: With PbI(OAc)2 In benzene at 0 - 25℃; for 8h; Further stages.; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
57% | Stage #1: trans-2-decene; 2,2,2-trichloroethyl sulfamate With tetra(trifluoroacetamidato)dirhodium(II); magnesium oxide In benzene at 0℃; Stage #2: With PbI(OAc)2 In benzene at 0 - 25℃; for 8h; Further stages.; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
65% | Stage #1: 1,2-Dihydronaphthalene; 2,2,2-trichloroethyl sulfamate With tetra(trifluoroacetamidato)dirhodium(II); magnesium oxide In benzene at 0℃; Stage #2: With [bis(acetoxy)iodo]benzene In benzene at 0 - 25℃; for 8h; Further stages.; | |
39% | With tetrakis(μ-trifluoroacetamidato)dirhodium(II); [bis(acetoxy)iodo]benzene; magnesium oxide In benzene at 0 - 25℃; for 8h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
85% | With [bis(acetoxy)iodo]benzene; magnesium oxide In chlorobenzene at -10 - 23℃; for 8h; | |
85% | Stage #1: cis-1-phenyl-1-propylene; 2,2,2-trichloroethyl sulfamate With tetra(trifluoroacetamidato)dirhodium(II); magnesium oxide In benzene at 0℃; Stage #2: With [bis(acetoxy)iodo]benzene In benzene at 0 - 25℃; for 8h; Further stages.; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
95% | Stage #1: 1-nitro-3-vinyl-benzene; 2,2,2-trichloroethyl sulfamate With tetra(trifluoroacetamidato)dirhodium(II); magnesium oxide In benzene at 0℃; Stage #2: With [bis(acetoxy)iodo]benzene In benzene at 0 - 25℃; for 8h; Further stages.; | |
With [bis(acetoxy)iodo]benzene; magnesium oxide In chlorobenzene at -10 - 23℃; for 8h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
79% | Stage #1: 2-bromostyrene; 2,2,2-trichloroethyl sulfamate With tetra(trifluoroacetamidato)dirhodium(II); magnesium oxide In benzene at 0℃; Stage #2: With [bis(acetoxy)iodo]benzene In benzene at 0 - 25℃; for 8h; Further stages.; | |
71% | With [bis(acetoxy)iodo]benzene; rhodium perfluorobutyramide; magnesium oxide In benzene at 5 - 20℃; for 10h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
54% | Stage #1: Methyl cinnamate; 2,2,2-trichloroethyl sulfamate With tetra(trifluoroacetamidato)dirhodium(II); magnesium oxide In chlorobenzene at -40℃; for 1h; Stage #2: With [bis(acetoxy)iodo]benzene In chlorobenzene at 25℃; Further stages.; | |
With [bis(acetoxy)iodo]benzene; magnesium oxide In chlorobenzene at -10 - 23℃; for 8h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
72% | Stage #1: tert-butyl((3,7-dimethyloct-6-en-1-yl)oxy)dimethylsilane; 2,2,2-trichloroethyl sulfamate With tetra(trifluoroacetamidato)dirhodium(II); magnesium oxide In benzene at 0℃; Stage #2: With [bis(acetoxy)iodo]benzene In benzene at 0 - 25℃; for 8h; Further stages.; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
55% | Stage #1: carbon disulfide; 2,2,2-trichloroethyl sulfamate With sodium hydroxide In water; N,N-dimethyl-formamide at 0 - 23℃; for 2.83333h; Stage #2: dimethyl sulfate In water; N,N-dimethyl-formamide at 0 - 23℃; for 3.16667h; | |
55% | Stage #1: carbon disulfide; 2,2,2-trichloroethyl sulfamate With sodium hydroxide In water; N,N-dimethyl-formamide at 0 - 25℃; for 2h; Inert atmosphere; Stage #2: dimethyl sulfate In water; N,N-dimethyl-formamide at 0 - 25℃; for 3h; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
91% | With [bis(acetoxy)iodo]benzene; magnesium oxide In chlorobenzene at -10 - 23℃; for 8h; | |
67% | With copper(l) iodide; iodosylbenzene In acetonitrile at 20℃; for 18h; Molecular sieve; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
70% | With [bis(acetoxy)iodo]benzene; magnesium oxide In chlorobenzene at -10 - 23℃; for 8h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
40% | With [bis(acetoxy)iodo]benzene; magnesium oxide In chlorobenzene at -10 - 23℃; for 8h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
85% | With [bis(acetoxy)iodo]benzene; magnesium oxide In chlorobenzene at -10 - 23℃; for 8h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
91% | With magnesium oxide In chlorobenzene at -10 - 23℃; for 8h; | |
91% | With tetrakis(μ-trifluoroacetamidato)dirhodium(II); magnesium oxide In chlorobenzene at 5 - 20℃; for 12h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With bis(tertbutylcarbonyloxy)iodobenzene In benzene at 23℃; | ||
Stage #1: (3-methylbutyl)benzene; 2,2,2-trichloroethyl sulfamate With bis{rhodium[3,3'-(1,3-phenylene)bis(2,2-dimethylpropanoic acid)]; 2-methyl-2-phenylpropionic acid; magnesium oxide In Isopropyl acetate for 0.0833333h; Molecular sieve; Inert atmosphere; Stage #2: With [bis(acetoxy)iodo]benzene In Isopropyl acetate for 12.5h; Molecular sieve; Inert atmosphere; | ||
With tert-butyl isocyanide; [bis(acetoxy)iodo]benzene; dirhodium(II) tetrakis[N-tetrafluorophthaloyl-(S)-tert-leucinate] at 20℃; for 16h; Overall yield = 57 percent; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
100% | With [bis(acetoxy)iodo]benzene; C32H44ClN4O4Rh2*3CH2Cl2 at 20℃; for 3h; Inert atmosphere; | |
95% | With bis(tertbutylcarbonyloxy)iodobenzene In benzene at 23℃; | |
64% | With bis{rhodium[3,3'-(1,3-phenylene)bis(2,2-dimethylpropanoic acid)]; [bis(acetoxy)iodo]benzene In water at 4℃; for 24h; |
18% | With [p-(trifluoromethyl)phenyl](diacetoxy)-λ3-bromane at 0 - 15℃; for 3h; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
46% | With bis(tertbutylcarbonyloxy)iodobenzene In benzene at 23℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
90% | With [bis(acetoxy)iodo]benzene; bis[rhodium(α,α,α',α'-tetramethyl-1,3-benzenedipropionic acid)]; sodium hydrogencarbonate; | Rh2 (esp) 2 (0.001 mmol, 0.7 6 mg), <strong>[100-41-4]ethylbenzene</strong> (0.3 mmol, 31.8 mg), 2,2,2-trichloroethylsulfamic acid in a 50-liter stainless steel mortar Ester (0.2 mmol, 45.7 mg), iodobenzene diacetate (0.4 mmol, 129 mg), NaHC03 (200 mg). Then place the stainless steel mortar on the ball mill (Miqi YXQM: -4L). After safely placing it, adjust the speed to 300r/min for 150min to start the machine. After completion of the reaction, the temperature was lowered to 25 C to 30 C, and dichloromethane was added to the reaction system, followed by washing 3 times. The above dichloromethane solution was washed three times with water, and the methylene chloride phase was dried over anhydrous sodium sulfate. Separation was carried out using a silica gel column of 100 to 200 mesh, eluting with a petroleum ether/ethyl acetate (20:1) mixed solvent, and the desired product 2,2,2-trichloroethyl(1-phenylethyl)amino group was collected. The sulfonate was concentrated, and the organic phase was concentrated under reduced pressure to remove solvent and dried in vacuo to afford white powder. The obtained product has the structural formula shown as 3, wherein: 1?1 = ?11-, 1?2=]^-, 1?3 = (:1 especially 012-. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
85% | With bis(tertbutylcarbonyloxy)iodobenzene In benzene-d6 for 100h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With bis(tertbutylcarbonyloxy)iodobenzene In benzene at 23℃; |
Tags: 69226-51-3 synthesis path| 69226-51-3 SDS| 69226-51-3 COA| 69226-51-3 purity| 69226-51-3 application| 69226-51-3 NMR| 69226-51-3 COA| 69226-51-3 structure
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H312 | Harmful in contact with skin |
H313 | May be harmful in contact with skin |
H314 | Causes severe skin burns and eye damage |
H315 | Causes skin irritation |
H316 | Causes mild skin irritation |
H317 | May cause an allergic skin reaction |
H318 | Causes serious eye damage |
H319 | Causes serious eye irritation |
H320 | Causes eye irritation |
H330 | Fatal if inhaled |
H331 | Toxic if inhaled |
H332 | Harmful if inhaled |
H333 | May be harmful if inhaled |
H334 | May cause allergy or asthma symptoms or breathing difficulties if inhaled |
H335 | May cause respiratory irritation |
H336 | May cause drowsiness or dizziness |
H340 | May cause genetic defects |
H341 | Suspected of causing genetic defects |
H350 | May cause cancer |
H351 | Suspected of causing cancer |
H360 | May damage fertility or the unborn child |
H361 | Suspected of damaging fertility or the unborn child |
H361d | Suspected of damaging the unborn child |
H362 | May cause harm to breast-fed children |
H370 | Causes damage to organs |
H371 | May cause damage to organs |
H372 | Causes damage to organs through prolonged or repeated exposure |
H373 | May cause damage to organs through prolonged or repeated exposure |
Environmental hazards | |
Code | Phrase |
H400 | Very toxic to aquatic life |
H401 | Toxic to aquatic life |
H402 | Harmful to aquatic life |
H410 | Very toxic to aquatic life with long-lasting effects |
H411 | Toxic to aquatic life with long-lasting effects |
H412 | Harmful to aquatic life with long-lasting effects |
H413 | May cause long-lasting harmful effects to aquatic life |
H420 | Harms public health and the environment by destroying ozone in the upper atmosphere |
Sorry,this product has been discontinued.
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