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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 704773생성일: 2026년 10월 25일

(3S,4R)-4-amino-3-hydroxy-2,2-dimethyl-chroman-6-carbonitrile → (3S,4R)-4-amino-3-hydroxy-2,2-dimethyl-chroman-6-carbonitrile

https://huagongshe.com/reaction/704773

반응식

참여 물질

역할이름HCID투입량
반응물(3S,4R)-4-amino-3-hydroxy-2,2-dimethyl-chroman-6-carbonitrileHCID 10943936—
반응물(-)-di(p-toluoyl)-L-tartaric acid monohydrateHCID 69630779—
용매EthanolHCID 702—
생성물(3S,4R)-4-amino-3-hydroxy-2,2-dimethyl-chroman-6-carbonitrileHCID 1094393622.3%
생성물Di-para-toluoyl-L-tartaric acidHCID 29414711—

반응 단계

A mixture of trans-4-amino-3,4-dihydro-2,2-dimethyl-3-hydroxy-2H-1-benzopyran-6-carbonitrile (193 g) and (-)-di-p-toluoyl-L-tartaric acid monohydrate (358 g) was dissolved in ethanol (600 ml) under reflux. The mixture was cooled to room temperature and stood for 3 days to give a white precipitate. This precipitate was collected by filtration, washed with a small volume of ethanol, and recrystallized twice from ethanol to give (-)-di-p-toluoyl-L-tartaric acid salt of (3S,4R)-4-amino-3,4-dihydro-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-6-carbonitrile (43.1 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04988723
출처 데이터셋uspto-grants-1991_01
ORD IDord-a9fa8379fc7944f0968f5a2d06b0cb30
출처 메모uspto-grants-1991_01