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HRID 704773作成日:2026年10月26日

(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

反応式

関与物質

役割名称HCID仕込み量
反応物(3S,4R)-4-amino-3-hydroxy-2,2-dimethyl-chroman-6-carbonitrileHCID 10943936—
反応物(-)-di(p-toluoyl)-L-tartaric acid monohydrateHCID 69630779—
溶媒EthanolHCID 702—
生成物(3S,4R)-4-amino-3-hydroxy-2,2-dimethyl-chroman-6-carbonitrileHCID 1094393622.3%
生成物Di-para-toluoyl-L-tartaric acidHCID 29414711—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04988723
出典データセットuspto-grants-1991_01
ORD IDord-a9fa8379fc7944f0968f5a2d06b0cb30
出典メモuspto-grants-1991_01