Water → HCID 13662974, compound
Reaction equation
[H-].[Na+].[CH3:3][O:4][C:5]([C:7]1[NH:8][C:9]2[C:14]([CH:15]=1)=[CH:13][CH:12]=[C:11]([CH3:16])[CH:10]=2)=[O:6].[C:17](Cl)(=[O:19])[CH3:18].O>CN(C)C=O>[CH3:3][O:4][C:5]([C:7]1[N:8]([C:17](=[O:19])[CH3:18])[C:9]2[C:14]([CH:15]=1)=[CH:13][CH:12]=[C:11]([CH3:16])[CH:10]=2)=[O:6]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
Sodium hydride (4.70 g. of 50% dispersion in mineral oil) was added portionwise with stirring to a stirred solution of 6-methylindole-2-carboxylic acid methyl ester (18.0 g.) in dry N,N-dimethylformamide (100 ml.) and the mixture was stirred at room temperature for 1.5 hours. Acetyl chloride (8.0 g.) was then added dropwise with stirring and cooling and the resulting mixture was stirred at room temperature for 5 hours and then poured into water. The mixture was extracted several times with ethyl acetate and the combined extracts were washed with water and dried (Na2SO4). Evaporation of the solvent gave an oil which was chromatographed on silica gel. Elution with chloroform first gave mineral oil followed by pure product. Evaporation of the product-containing fractions gave a solid which crystallized from methanol to give 1-acetyl-6-methylindole-2-carboxylic acid methyl ester (14.4 g.), m.p. 51°-53° C.
Workup
- stirringwith stirring
- temperaturecooling
- stirringthe resulting mixture was stirred at room temperature for 5 hours
- extractionThe mixture was extracted several times with ethyl acetate
- washthe combined extracts were washed with water
- dry with materialdried (Na2SO4)
- customEvaporation of the solvent
- customgave an oil which
- customwas chromatographed on silica gel
- washElution with chloroform first gave mineral oil
- customEvaporation of the product-containing fractions
- customgave a solid which
- customcrystallized from methanol
Sources & evidence
- ORD record
- ord-bb1b25c090b54be78cc16486bb71a741
- Source dataset
- uspto-grants-1983_10
- Patent number
- US04410539
Reaction notes
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