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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 247462생성일: 2026년 10월 25일

Water → 2-[(7-Methoxy-1,2,3,4-tetrahydronaphth-2-yl)amino]-1-phenylethanol hydrochloride

https://huagongshe.com/reaction/247462

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물PhenylglyoxalHCID 14090—
반응물Sodium borohydrideHCID 4311764—
반응물7-Methoxy-1,2,3,4-tetrahydronaphthalen-2-amine hydrochlorideHCID 14750915—
용매MethanolHCID 887—
생성물2-[(7-Methoxy-1,2,3,4-tetrahydronaphth-2-yl)amino]-1-phenylethanol hydrochlorideHCID 2016088520%

반응 조건

온도4 °C

반응 단계

An amount of 3.53 g of phenylglyoxal is reacted under stirring at room temperature for 3 hours with 5 g of 2-amino-7-methoxy-1,2,3,4-tetrahydronaphthalene hydrochloride in 100 ml of methanol in the presence of 0.9 g of sodium borohydride. After cooling to 4° C., 4,3 g of sodium borohydride are added and the reacting mixture is left under stirring at room temperature for a night. After addition of 20 ml of water, the solution is stirred at room temperature for 15 minutes, then it is evaporated to dryness. The residue is dissolved in 300 ml of ethyl acetate and 60 ml of water; after filtration, the organic phase is separated, dried over magnesium sulfate, filtered and evaporated to dryness. The oil thus obtained is purified by flash-chromatography by using a mixture ethyl acetate/methanol 8/2 as eluant to obtain the 2-[(7-methoxy-1,2,3,4-tetrahydronaphth-2-yl)amino]-1-phenylethanol hydrochloride. Yield: 20% of the theoretical value.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04707497
출처 데이터셋uspto-grants-1987_11
ORD IDord-a395cc8371f745c7a98988b156bd69c4
출처 메모uspto-grants-1987_11