Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Allyl bromide → N-(4-chlorophenyl)-1-(2-propenyl)-4-piperidinamine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Allyl bromide | HCID 7841 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | N-(4-chlorophenyl)piperidin-4-amine | HCID 7183033 | — |
| 용매 | Benzene | HCID 241 | — |
| 생성물 | N-(4-chlorophenyl)-1-(2-propenyl)-4-piperidinamine | HCID 23339007 | — |
반응 단계
To a stirred mixture of 15 parts of N-(4-chlorophenyl)-4-piperidinamine, 12 parts of N,N-diethylethanamine in 130 parts of benzene is added dropwise a solution of 10.3 parts of 3-bromo-1-propene in 70 parts of benzene. Upon completion, the whole is stirred first for 20 h. 30 at room temperature and further for 40 minutes at reflux. The reaction mixture is cooled, filtered and the filtrate is evaporated. The residue is taken up in 1,1'-oxybisethane and treated with activated charcoal. The latter is filtered off and the 1,1'-oxybisethane is evaporated again, yielding 2.9 parts of N-(4-chlorophenyl)-1-(2-propenyl)-4-piperidinamine; mp. 90° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04225606 |
| 출처 데이터셋 | uspto-grants-1980_09 |
| ORD ID | ord-892bec6fc0e0497e96b6d153d36e6999 |
| 출처 메모 | uspto-grants-1980_09 |