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HRID 404714作成日:2026年10月26日

4-Bromobenzaldehyde → N-(4-Bromobenzyl)-2,2-dimethoxyethanamine

https://huagongshe.com/reaction/404714

反応式

関与物質

役割名称HCID仕込み量
反応物4-BromobenzaldehydeHCID 70741—
反応物Aminoacetaldehyde dimethyl acetalHCID 89728—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
反応物Sodium borohydrideHCID 4311764—
溶媒Acetic AcidHCID 176—
溶媒TolueneHCID 1140—
生成物N-(4-Bromobenzyl)-2,2-dimethoxyethanamineHCID 5922624181.7%

反応手順

50 g (270.2 mmol) 4-bromobenzaldehyde were dissolved in 200 ml of toluene and 28.4 g (270.2 mmol) aminoacetaldehyde dimethylacetal were added. After the addition of 5.1 g (27.0 mmol) p-toluenesulfonic acid monohydrate, the reaction mixture was heated under reflux in a Dean Stark apparatus. After 4 h, the reaction was cooled to room temperature and washed with saturated sodium hydrogen carbonate-solution (2×) and water. The combined aqueous layers were extracted with Toluene and the combined organic layers were dried over magnesium sulfate and evaporated. The residue was dissolved in 200 ml of ethanol and 5.11 g (135.1 mmol) of sodium borohydride were added in small portions. After stirring for 2 h at room temperature and standing overnight, 5.0 ml acetic acid were added and the solvent was removed i. vac. The residue was taken up in dichloromethane and washed (2×) with water. After drying over magnesium sulfate and evaporation, 60.5 g of the title compound were obtained (crude product), which were used without further purification. Rt=0.80 min (Method C). Detected mass: 274.1/276.1 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08748614B2
出典データセットuspto-grants-2014_06
ORD IDord-5d4402caa3d54c78a237de7453d9ab3a
出典メモuspto-grants-2014_06