Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
3-Piperidinone, 1-(phenylmethyl)- → 4-(1-Benzylpiperidin-3-yliden)-butyronitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 3-Piperidinone, 1-(phenylmethyl)- | HCID 96650 | — |
| 반응물 | (3-Cyanopropyl)triphenylphosphonium bromide | HCID 3036619 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 4-(1-Benzylpiperidin-3-yliden)-butyronitrile | HCID 53987194 | — |
반응 단계
77.3 g (188.3 mmol) 3-cyanopropyl-triphenylphosphonium bromide are suspended in 300 ml toluene and added to 22.0 g (191.9 mmol) potassium tert-butylate. The mixture is cooled to ca 0° C. under moisture exclusion and a solution of 34.6 g (182.8 mmol) 1-benzyl-3-piperidone in 50 ml toluene is added dropwise under cooling. The batch is left to stand overnight at ca. 0° C. and subsequently diluted with 200 ml toluene and washed twice, each with 100 ml water. The organic phase is extracted with 150 ml half concentrated hydrochloric acid. Subsequently, the aqueous phase is made basic with 200 ml 10% sodium hydroxide solution and extracted twice, each with 250 ml toluene.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07241745B2 |
| 출처 데이터셋 | uspto-grants-2007_07 |
| ORD ID | ord-3f7745a5be8c402ab5eab096d3914222 |
| 출처 메모 | uspto-grants-2007_07 |