Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1730626생성일: 2026년 10월 27일
1,2,3,6-Tetrahydrophthalimide → 2-Octadecanoyl-3a,4,7,7a-tetrahydro-1H-isoindole-1,3(2H)-dione
https://huagongshe.com/reaction/1730626
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,2,3,6-Tetrahydrophthalimide | HCID 6808 | — |
| 반응물 | Stearoyl chloride | HCID 8212 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Triethylamine hydrochloride | HCID 11130 | — |
| 용매 | 1,1-Dichloropropane | HCID 6573 | — |
| 생성물 | 2-Octadecanoyl-3a,4,7,7a-tetrahydro-1H-isoindole-1,3(2H)-dione | HCID 21495916 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US03993640 |
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| 출처 데이터셋 | uspto-grants-1976_11 |
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| ORD ID | ord-50c53ed3456541ea802fb9d37c9a3ce0 |
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| 출처 메모 | uspto-grants-1976_11 |
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