Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → 1-Benzyl-3-(2-chloroethyl-methyl-amino)-pyrrolidine-2,5-dione
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Benzylmaleimide | HCID 74204 | — |
| 반응물 | Ethanamine, 2-chloro-N-methyl-, hydrochloride (1:1) | HCID 3028223 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 1-Benzyl-3-(2-chloroethyl-methyl-amino)-pyrrolidine-2,5-dione | HCID 15069998 | — |
반응 단계
74.8 g (0.4 mol) of N-benzylmaleimide [Arch. Pharm. 308, 489 (1975)] and 52.0 g (0.4 mol) of 2-chloroethyl-methylamine hydrochloride are initially introduced into 400 ml of dioxane and 40.4 g (0.4 mol) of triethylamine are added dropwise at 20° C. The mixture is then boiled under reflux for 5 hours. The batch is subsequently poured into 2 l of ice-water and extracted with 3 portions of 400 ml of chloroform and the extract is washed with water, dried over sodium sulphate and concentrated on a rotary evaporator. Chromatography of the residue (101.1 g) on silica gel using ethyl acetate:petroleum ether (1:2) gives 56.8 g (51% of theory) of an oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05416096 |
| 출처 데이터셋 | uspto-grants-1995_05 |
| ORD ID | ord-da47da9dd3b24d709e30733c6934b70e |
| 출처 메모 | uspto-grants-1995_05 |