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HRID 1054663作成日:2026年10月25日

Hydrochloric Acid → 6-chloro-5-(3,4-dimethoxyphenyl)-1H-indole-3-carboxylic acid

https://huagongshe.com/reaction/1054663

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物MethanolHCID 887—
反応物Sodium HydroxideHCID 14798—
反応物methyl 6-chloro-5-(3,4-dimethoxyphenyl)-1H-indole-3-carboxylateHCID 86698666—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物6-chloro-5-(3,4-dimethoxyphenyl)-1H-indole-3-carboxylic acidHCID 8669866724%

反応手順

A solution of methyl 6-chloro-5-(3,4-dimethoxyphenyl)-1H-indole-3-carboxylate (75 mg, 0.22 mmol), methanol (2.2 mL), and aqueous sodium hydroxide (1 M, 0.75 mL, 0.75 mmol) was heated at 75° C. for 24 hours. The reaction was acidified with 1 M HCl to pH=2 then diluted with ethyl acetate. The aqueous layer was back-extracted twice with ethyl acetate. The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo to provide a crude solid. The crude product was dissolved in methylene chloride and methanol and silica gel was added. The solvent was removed in vacuo and the crude material adsorbed onto silica was loaded onto a column of silica gel and eluted with ethyl acetate (with 0.2% formic acid)/heptanes (1:1 to 1:0) to provide the title compound (17 mg, 24%) as a tan solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09394285B2
出典データセットuspto-grants-2016_07
ORD IDord-ecc5855cb67847c38ba53629fdd16862
出典メモuspto-grants-2016_07