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HRID 371227作成日:2026年10月27日

2,4-Dimethoxybenzylamine hydrochloride → 2,4-Dimethoxybenzylamine

https://huagongshe.com/reaction/371227

反応式

関与物質

役割名称HCID仕込み量
反応物2,4-Dimethoxybenzylamine hydrochlorideHCID 3084343—
溶媒Sodium HydroxideHCID 14798—
生成物2,4-DimethoxybenzylamineHCID 597250103.5%

反応手順

12.0 g of 2,4-dimethoxybenzylamine hydrochloride is added to 100 ml of 1N sodium hydroxide solution and the mixture is extracted with 125 ml of ethyl acetate. The organic layer is dried over anhydrous sodium sulfate and stripped of solvent to give 10.2 g of 2,4-dimethoxybenzylamine as an oil. This amine is dissolved in 150 ml of benzene; 6.47 g of benzaldehyde and 0.6 g of p-toluenesulfonic acid monohydrate are added. The mixture is heated under reflux removing water with a Dean-Stark separator and in two hours the calculated amount of water (1.1 ml) separates out. The mixture is cooled to room temperature. Upon further cooling the benzene solution deposits some precipitate. Benzene is removed under reduced pressure and 60 ml of petroleum ether is added to the residue. An oily layer separates out with more precipitate. Benzene (10 ml) is added to make the layers homogeneous and the remaining precipitate is filtered. The filtrate is stripped of solvent to give 14.2 g of the title compound as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04529698
出典データセットuspto-grants-1985_07
ORD IDord-85dafb4b281548cfa10c2e8c27bbd534
出典メモuspto-grants-1985_07