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HRID 1284450作成日:2026年10月26日

Benzoyl chloride → (3S)-2-benzoyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

https://huagongshe.com/reaction/1284450

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoyl chlorideHCID 7412—
反応物Sodium HydroxideHCID 14798—
反応物boric acid, sodium saltHCID 159383—
反応物(3S)-6,7-Dihydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acidHCID 12926159—
溶媒WaterHCID 962—
生成物(3S)-2-benzoyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acidHCID 1393580982.1%

反応手順

(3S)-6,7-Dihydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid [J. Org. Chem., 26, 3533 (1961)] (33.9 g) and sodium borate.10H2O (62 g) are suspended in water (500 ml). Benzoyl chloride (27.5 g) and a solution of sodium hydroxide (13 g) in water (100 ml) are added dropwise to the suspension at 0° C. under stirring. The mixture is stirred at room temperature for 4 hours. The mixture is washed with ethyl acetate, and acidified with conc. HCl, and extracted with ethyl acetate. The extract is dried and distilled to remove the solvent. The crystals are collected by filtration, washed with benzene and then recrystallized from water, whereby (3S)-2-benzoyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (41.7 g) is obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04563306
出典データセットuspto-grants-1986_01
ORD IDord-9bd13a5707174b40aebb5d4118cc000c
出典メモuspto-grants-1986_01