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CAS No. : | 4741-58-6 | MDL No. : | MFCD00126369 |
Formula : | C10H10O4 | Boiling Point : | 404.2±45.0°C at 760 mmHg |
Linear Structure Formula : | - | InChI Key : | - |
M.W : | 194.18 g/mol | Pubchem ID : | - |
Synonyms : |
|
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: |
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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 |
---|---|---|
With nitric acid |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With acetic acid; zinc |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multistep reaction; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Yield given. Multistep reaction; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
20% | With sodium ethanolate In diethyl ether for 10h; Ambient temperature; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With N-Bromosuccinimide |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With magnesium oxide; trifluoroacetic acid; lithium chloride; palladium dichloride; thallium(III) trifluoroacetate 1.) THF, 25 deg C, 18 h, 2.) MeOH, room temperature, overnight; Yield given. Multistep reaction; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
78% | With potassium carbonate In N,N-dimethyl-formamide at 50℃; for 60h; | |
77% | With sodium methylate In methanol at 25℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With potassium hydroxide In methanol; water Heating; Yield given; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With n-butyllithium 1.) n-hexane, THF, -45 deg C, 2 h, 2.) a) n-hexane, THF, -45 deg C, 1 h, b) RT, overnight; Yield given. Multistep reaction; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Narkotinogendiol-metho-hydroxid, aq. KOH, Δ (neben 6-Methoxy-4,5-methylendioxy-2-vinyl-1-dimethylamino-benzol); | ||
aus Isobenzofuranon 16, CH2N2; | ||
Hydrastindiol-methjodid, sd. NaOH (neben N,N-Dimethyl-2-methoxy-3,4-methylendioxy-6-vinyl-benzylamin od. der methoxylfreien Verb.); |
Narcotindiol-methjodid, sd. NaOH (neben N,N-Dimethyl-2-methoxy-3,4-methylendioxy-6-vinyl-benzylamin od. der methoxylfreien Verb.); | ||
monomeres u. polymeres 2-Hydroxymethyl-3,4-dimethoxy-benzaldehyd, 40percent-ig. KOH, Δ, Dampfbad; | ||
aus (+-)-Alpinigenin-diol (XXI), MnO2; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With sodium hydroxide |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With hydrogenchloride; tin Behandeln der filtrierten Loesung mit Natriumnitrit und Ansaeuern mit Salzsaeure; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With sodium amalgam; sodium carbonate |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
at 20℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Versetzen mit Saeure; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
at 150 - 155℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Electrolysis; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Electrolysis; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: 67 percent / iodine, silver trifluoroacetate / CHCl3 2: 78 percent / potassium carbonate / PdCl2(PPh3)2 / dimethylformamide / 60 h / 50 °C / 3040 Torr |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: dimethylformamide / 0.5 h / 110 °C 2: potassium hydroxyde / H2O; methanol / Heating |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 4 steps 2: 99 percent / pyridine / benzene / 1 h / Heating 3: 74 percent / 1,8-diazabicylo<5.4.0>undec-7-ene (DBU) / benzene / 1 h / Heating 4: 81 percent / BBr3 / CH2Cl2 / 1.) 0 deg C, 30 min, 2.) RT, 3 h |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 3 steps 2: 99 percent / pyridine / benzene / 1 h / Heating 3: 4 percent / 1,8-diazabicylo<5.4.0>undec-7-ene (DBU) / benzene / 1 h / Heating |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 3 steps 2: 99 percent / pyridine / benzene / 1 h / Heating 3: 74 percent / 1,8-diazabicylo<5.4.0>undec-7-ene (DBU) / benzene / 1 h / Heating |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 2: 99 percent / pyridine / benzene / 1 h / Heating |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: NBS 2: 55 percent / triethylamine / acetone / 96 h / Ambient temperature |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 3 steps 1: NBS 2: 55 percent / triethylamine / acetone / 96 h / Ambient temperature 3: trifluoroacetic acid / CH2Cl2 / Ambient temperature |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: aqueous nitric acid 2: ethanol |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
64% | Stage #1: terephthalaldehyde, With palladium 10% on activated carbon; sodium carbonate In isopropyl alcohol at 120℃; for 24h; Inert atmosphere; Stage #2: 2-bromomethyl-1-iodo-4,5-dimethoxybenzene With triphenylphosphine In 1-methyl-pyrrolidin-2-one at 100℃; for 24h; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
1: 50% 2: 42% | With silver hexafluoroantimonate; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2 In dichloromethane at 160℃; for 72h; Inert atmosphere; Sealed tube; regioselective reaction; |
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