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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 404714생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/404714

반응식

참여 물질

역할이름HCID투입량
반응물4-BromobenzaldehydeHCID 70741—
반응물Aminoacetaldehyde dimethyl acetalHCID 89728—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
반응물Sodium borohydrideHCID 4311764—
용매Acetic AcidHCID 176—
용매TolueneHCID 1140—
생성물N-(4-Bromobenzyl)-2,2-dimethoxyethanamineHCID 5922624181.7%

반응 단계

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+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08748614B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-5d4402caa3d54c78a237de7453d9ab3a
출처 메모uspto-grants-2014_06