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HRID 2142作成日:2026年10月23日

Triethylamine → N-(3,4-Dimethoxybenzenesulphonyl)-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/ja/reaction/2142

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物1,2,3,4-TetrahydroquinolineHCID 69460—
反応物3,4-Dimethoxybenzenesulfonyl chlorideHCID 2734183—
溶媒DichloromethaneHCID 6344—
生成物N-(3,4-Dimethoxybenzenesulphonyl)-1,2,3,4-tetrahydroquinolineHCID 667562—

反応手順

1,2,3,4-Tetrahydroquinoline (0.29 ml) was added to a suspension of 3,4-dimethoxybenzene sulphonyl chloride (0.50 g) in dichloromethane (15 ml) at room temperature. Triethylamine (0.44 ml) was added and the resulting mixture stirred for 24 hours at room temperature. The reaction mixture was then diluted with dichloromethane (20 ml) and washed successively with saturated aqueous sodium hydrogen carbonate solution (10 ml), 2N hydrochloric acid (10 ml) and saturated aqueous sodium chloride solution (10 ml). Drying over magnesium sulphate and concentration in vacuo provided a yellow oil. Purification by column chromatography eluting with 30% ethyl acetate in hexane provided the title compound as a colourless oil (0.60 g) which solidified on standing.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728712
出典データセットuspto-grants-1998_03
ORD IDord-80b4d3c6a338477cbce6e4a97e49acd8
出典メモuspto-grants-1998_03