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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1026783생성일: 2026년 10월 27일

Toluene → (2S,3R)-3-(3-Amino-phenyl)-1-(dimethylamino)-2-methyl-pentan-3-ol

https://huagongshe.com/reaction/1026783

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Ammonium bisulfateHCID 24655—
반응물(S)-3-(dimethylamino)-2-methyl-1-(3-nitro-phenyl)-propan-1-oneHCID 53235125—
반응물HCID 178418443HCID 178418443—
용매TetrahydrofuranHCID 8028—
생성물(2S,3R)-3-(3-Amino-phenyl)-1-(dimethylamino)-2-methyl-pentan-3-olHCID 7066450461.2%

반응 단계

726 ml of ethylmagnesium bromide (1M in THF; 0.726 mol) are added under a nitrogen flow into a 2-liter four-neck flask, provided with mechanical stirrer, thermometer and dropping funnel. A solution of (S)-3-(dimethylamino)-2-methyl-1-(3-nitro-phenyl)-propan-1-one (50 g, 0.242 mol) in 50 ml of THF are dripped maintaining the temperature between 15-30° C. The reaction is stirred at room temperature for 3 hours. It is cooled to about 10° C. and toluene (200 ml) and slowly a 20% ammonium hydrogen sulphate solution (200 ml) are added. The mixture is stirred for 30 minutes and the phases are separated after about 15 minutes of rest. The organic phase is concentrated under vacuum almost to oily residue. Then toluene (200 ml), 30% sodium metabisulfite solution (300 ml) are added. The mixture is stirred for 30 minutes and the phases are separated after about 15 minutes of rest. The aqueous phase is washed 2 times with 200 ml of toluene. The organic phases are eliminated while Cert-butylmethylether (200 ml) is added to the aqueous phase. The pH of the mixture is brought to 11-12 with 28% sodium hydroxide. The mixture is stirred for 30 minutes and the phases are separated after about 15 minutes of rest. The aqueous phase is eliminated while the organic phase is concentrated under vacuum to oily residue which solidifies by cooling. 35 g of a yellowish solid with a 95% HPLC purity are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08729308B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-2be645676eda4e9e9986508764467296
출처 메모uspto-grants-2014_05