Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Propyltriphenylphosphonium bromide → 1-Carbobenzoxy-4-(1-butylidene)piperidine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Propyltriphenylphosphonium bromide | HCID 80374 | — |
| 반응물 | Benzyl 4-oxopiperidine-1-carboxylate | HCID 643496 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-Carbobenzoxy-4-(1-butylidene)piperidine | HCID 20522020 | — |
반응 단계
Butyl lithium (44 ml of 1.6 M in hexane) was added slowly to a stirred suspension of 27 g of (n-propyl)triphenylphosphonium bromide in 350 ml of tetrahydrofuran and the resulting solution was refluxed for 1 hour. The mixture was cooled in an ice bath and 18 g of N-carbobenzyloxy-4-piperidone was added. After stirring at room temperature of 0.5 hour, the solution was refluxed for 2 hours. The cooled mixture was concentrated under reduced pressure, partitioned between ether and water, and the ether layer was dried (sodium sulfate) and evaporated. The residue was filtered through silica gel with 20% ethyl acetate-hexane to give 10 g of 1-carbobenzoxy-4-(1-butylidene)piperidine as a colorless oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04353901 |
| 출처 데이터셋 | uspto-grants-1982_10 |
| ORD ID | ord-f068b0d416624defa98b220467acb3f2 |
| 출처 메모 | uspto-grants-1982_10 |