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[ CAS No. 1261478-26-5 ] {[proInfo.proName]}

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Chemical Structure| 1261478-26-5
Chemical Structure| 1261478-26-5
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Product Details of [ 1261478-26-5 ]

CAS No. :1261478-26-5 MDL No. :MFCD18399428
Formula : C9H7F3O3 Boiling Point : -
Linear Structure Formula :- InChI Key :WYAZXWRYHRTDET-UHFFFAOYSA-N
M.W : 220.15 Pubchem ID :70874124
Synonyms :

Safety of [ 1261478-26-5 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 1261478-26-5 ]

* 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.

  • Downstream synthetic route of [ 1261478-26-5 ]

[ 1261478-26-5 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 1261478-26-5 ]
  • [ 2295968-21-5 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: di-isopropyl azodicarboxylate; triphenylphosphine / N,N-dimethyl-formamide / 3 h / 0 °C / Inert atmosphere 2: lithium hydroxide monohydrate / methanol; water / 3 h / 20 °C
  • 2
  • [ 1261478-26-5 ]
  • [ 2295966-54-8 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: di-isopropyl azodicarboxylate; triphenylphosphine / N,N-dimethyl-formamide / 3 h / 0 °C / Inert atmosphere 2: lithium hydroxide monohydrate / methanol; water / 3 h / 20 °C 3: pyridine; trichlorophosphate / 0.5 h / 0 °C
  • 3
  • [ 1261478-26-5 ]
  • [ 2295967-50-7 ]
  • [ 2295968-20-4 ]
YieldReaction ConditionsOperation in experiment
79% With di-isopropyl azodicarboxylate; triphenylphosphine In N,N-dimethyl-formamide at 0℃; for 3h; Inert atmosphere; 32.2 [00344] To a mixture of Example 32b (670 mg, 3.05 mmol), Example 32c (710 mg, 3.05 mmol), PPh3 (1.18 g, 4.5 mmol) was added dried DMF (15 mL), and the mixture was degassed for N2 protection. Then, DIAD (1.23 g) was injected into the mixture at 0°C dropwise, and the reaction solution was stirred for 3 h. After extraction with EtOAc (10 mL*2),the combined organic layer was dried over Na2S04,filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography (DCM/MeOH = 95/5) to give the desired product Example 32d (1.05 g, yield 79%) ascolorless oil.LCMS [M+l]+ = 436.0
  • 4
  • [ 67-56-1 ]
  • [ 79427-88-6 ]
  • [ 1261478-26-5 ]
YieldReaction ConditionsOperation in experiment
81% With thionyl chloride at 0 - 65℃; for 5h; 32.1 [00343] To the solution of Example 32a (900 mg, 4.37 mmol) in Me OH (20 mL) at 0°C was added SOCl2 (1 mL), and the mixture was heated at 65°C for 5 h. After the temperature was cooled down to r.t., it was concentrated under reduced pressure. The residue was purified by silica gel chromatography (pure petroleum ether) to give the desired product Example 32b (780 mg, yield 81%) as colorless liquid.
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Technical Information

• Acidity of Phenols • Acyl Group Substitution • Alcohols Convert Acyl Chlorides into Esters • Alcoholysis of Anhydrides • Alkyl Halide Occurrence • Amines Convert Esters into Amides • An Alkane are Prepared from an Haloalkane • Benzylic Oxidation • Birch Reduction • Birch Reduction of Benzene • Blanc Chloromethylation • Bouveault-Blanc Reduction • Catalytic Hydrogenation • Chan-Lam Coupling Reaction • Claisen Condensations Produce β-Dicarbonyl Compounds • Claisen Condensations Produce β-Dicarbonyl Compounds • Complete Benzylic Oxidations of Alkyl Chains • Complete Benzylic Oxidations of Alkyl Chains • Complex Metal Hydride Reductions • Conjugate Additions of p-Benzoquinones • Conversion of Amino with Nitro • Convert Esters into Aldehydes Using a Milder Reducing Agent • Decarboxylation of 3-Ketoacids Yields Ketones • Decomposition of Arenediazonium Salts to Give Phenols • Deprotection of Cbz-Amino Acids • Deprotonation of Methylbenzene • Diazo Coupling • Directing Electron-Donating Effects of Alkyl • Electrophilic Chloromethylation of Polystyrene • Electrophilic Substitution of the Phenol Aromatic Ring • Ester Cleavage • Ester Hydrolysis • Etherification Reaction of Phenolic Hydroxyl Group • Friedel-Crafts Alkylation of Benzene with Acyl Chlorides • Friedel-Crafts Alkylation of Benzene with Carboxylic Anhydrides • Friedel-Crafts Alkylation of Benzene with Haloalkanes • Friedel-Crafts Alkylation Using Alkenes • Friedel-Crafts Alkylations of Benzene Using Alkenes • Friedel-Crafts Alkylations Using Alcohols • Friedel-Crafts Reaction • Grignard Reagents Transform Esters into Alcohols • Groups that Withdraw Electrons Inductively Are Deactivating and Meta Directing • Halogenation of Benzene • Halogenation of Phenols • Hantzsch Pyridine Synthesis • Hydrogenation to Cyclohexane • Hydrogenolysis of Benzyl Ether • Ketones Undergo Mixed Claisen Reactions to Form β-Dicarbonyl Compounds • Kolbe-Schmitt Reaction • Nitration of Benzene • Nucleophilic Aromatic Substitution • Nucleophilic Aromatic Substitution with Amine • Oxidation of Alkyl-substituted Benzenes Gives Aromatic Ketones • Oxidation of Phenols • Pechmann Coumarin Synthesis • Preparation of Aldehydes and Ketones • Preparation of Alkylbenzene • Reactions of Benzene and Substituted Benzenes • Reactions with Organometallic Reagents • Reduction of an Ester to an Alcohol • Reduction of an Ester to an Aldehyde • Reductive Removal of a Diazonium Group • Reimer-Tiemann Reaction • Reverse Sulfonation——Hydrolysis • Specialized Acylation Reagents-Carbodiimides and Related Reagents • Sulfonation of Benzene • The Acylium Ion Attack Benzene to Form Phenyl Ketones • The Claisen Rearrangement • The Cycloaddition of Dienes to Alkenes Gives Cyclohexenes • The Nitro Group Conver to the Amino Function • Transesterification • Vilsmeier-Haack Reaction
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