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HRID 1730626作成日:2026年10月27日

1,2,3,6-Tetrahydrophthalimide → 2-Octadecanoyl-3a,4,7,7a-tetrahydro-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/1730626

反応式

関与物質

役割名称HCID仕込み量
反応物1,2,3,6-TetrahydrophthalimideHCID 6808—
反応物Stearoyl chlorideHCID 8212—
反応物TriethylamineHCID 8471—
反応物Triethylamine hydrochlorideHCID 11130—
溶媒1,1-DichloropropaneHCID 6573—
生成物2-Octadecanoyl-3a,4,7,7a-tetrahydro-1H-isoindole-1,3(2H)-dioneHCID 21495916—

反応手順

A solution of 4-cyclohexene-1,2-dicarboximide (151g) and triethylamine (300 mls) in dichloropropane (900 mls) was maintained at a temperature of 50° C during the addition thereto over a period of 10 minutes, with constant stirring, of a solution of stearoyl chloride (302.5g) in a dichloropropane (300 mls). The mixture was stirred at 50° C for a further period of 10 minutes during which time triethylamine hydrochloride precipitated out, and was then filtered hot. The filtered precipitate was then washed with small portions of hot dichloropropane and the washings were combined with the filtrate. The solvent from the combined washings and filtrate was then evaporated off in a rotary evaporator to yield solid N-stearoyl-4-cyclohexene-1,2-dicarboximide, which was recrystallised from 60° - 80° petroleum ether.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03993640
出典データセットuspto-grants-1976_11
ORD IDord-50c53ed3456541ea802fb9d37c9a3ce0
出典メモuspto-grants-1976_11