戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 465908作成日:2026年10月26日

Hydrochloric Acid → 2,4-Dimethoxybenzoic acid

https://huagongshe.com/reaction/465908

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Chloromethyl Methyl EtherHCID 7864—
反応物Sodium HydroxideHCID 14798—
反応物4-Methoxysalicylic AcidHCID 75231—
反応物DiisopropylethylamineHCID 81531—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物2,4-Dimethoxybenzoic acidHCID 7052114.9%

反応手順

12.05 g of 4-methoxysalicylic acid was dispersed in 200 ml of methylene chloride in argon atmosphere. To the dispersion were added 27.70 g of N,N-diisopropylethylamine and 19.20 g of chloromethylmethyl ether, and the mixture was agitated for 42 hours. The reaction mixture was poured into water, and extracted with methylene chloride. The extract was dried over anhydrous sodium sulfate. The solvent was distilled off in evacuated atomosphere, and 300 ml of methanol was added to the residue. To the mixture was added a solution which has been prepared by dissolving 8.50 g of sodium hydroxide in 20 ml of water. The mixture was agitated for 20 hours, neutralized with 6N aqueous hydrochloric acid, and the solvent was distilled off in evacuated atomosphere. The mixture was adjusted to pH 1 with 1N aqueous hydrochloric acid, and extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and the solvent was distilled off in evacuated atomosphere to produce 15 g of 4-methoxy-2-methoxy benzoic acid. To the product were added 8.50 g of 2-mercaptothiazoline, 15.34 g of N,'N-dicyclohexylcarbodiimide, 0.86 g of 4-dimethylaminopyridine, and 400 ml of 1,2-dichloroethane, and the mixture was agitated for 18 hours. The reaction mixture was filtered and the precipitate was washed with benzene. The filtrate and the wash liquid were combined, washed with 2N aqueous solution of sodium hydroxide, water, and saturated aqueous solution of sodium chloride in this order, and dried over anhydrous sodium sulfate. The solvent was distilled off in evacuated atomosphere, and the residue was subjected to a column chromatography using silica gel. There was obtained 12.36 g of N-(4-methoxy-2-methoxymethoxybenzoyl)thiazolidine-2-thion from fractions eluted with methylene chloride.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05155106
出典データセットuspto-grants-1992_10
ORD IDord-5eb94eee4a2949b18573ae508562052a
出典メモuspto-grants-1992_10