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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1772생성일: 2026년 10월 24일

Water → 5-Chloro-alpha-(2-chlorophenyl)-2-(2,4-dimethoxybenzyl)aminobenzyl alcohol

https://huagongshe.com/ko/reaction/1772

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2,4-DimethoxybenzaldehydeHCID 69175—
반응물Sodium borohydrideHCID 4311764—
반응물(2-Amino-5-chlorophenyl)(2-chlorophenyl)methanolHCID 11437092—
용매Acetic AcidHCID 176—
생성물5-Chloro-alpha-(2-chlorophenyl)-2-(2,4-dimethoxybenzyl)aminobenzyl alcoholHCID 5384149596.1%

반응 단계

To a solution of 2-amino-5-chloro-α-(2-chloro phenyl)benzyl alcohol (5.0 g) and 2,4-dimethoxy benzaldehyde (3.72 g) in acetic acid (50 ml) was added, under ice-cooling, sodium borohydride (0.94 g). The mixture was stirred for one hour at room temperature, which was poured into water (200 ml), followed by extraction with ethyl acetate (200 ml×2). The ethyl acetate layer was washed with 1N sodium hydroxide, which was dried over anhydrous magnesium sulfate, followed by distilling off the solvent under reduced pressure. The residue was purified by means of a silica gel column chromatography (hexane:ethyl acetate=5:1) to give 5-chloro-α-(2-chlorophenyl)-2-(2,4-dimethoxybenzyl)aminobenzyl alcohol (7.5 g) as an oily product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726306
출처 데이터셋uspto-grants-1998_03
ORD IDord-8208d819f879448fbecf7d2aa5f1ad04
출처 메모uspto-grants-1998_03