Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Formic Acid → ethyl (3R)-1-methylpiperidine-3-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Formic Acid | HCID 284 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | ethyl (3R)-piperidine-3-carboxylate | HCID 185582 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 용매 | Formaldehyde | HCID 712 | — |
| 생성물 | ethyl (3R)-1-methylpiperidine-3-carboxylate | HCID 736036 | 73% |
반응 단계
(R)-Ethyl nipecotate (5.7 g 365 mmol), (prepared by resolution of ethyl nipecotate by treatment with L(+)-tartaric acid as described in J. Org. Chem. 1991, (56), 1168), was dissolved in 38.5% aqueous formaldehyde solution (45 ml) and formic acid (90 ml) and the mixture heated at reflux for 18 hours. The mixture was allowed to cool and added dropwise to cooled saturated aqueous sodium hydrogen carbonate solution. The mixture was adjusted to pH12 by addition of sodium hydroxide and the mixture was extracted with methylene chloride. The organic extract was washed with brine, dried (MgSO4) and the solvent removed by evaporation to give (R)-ethyl 1-methylpiperidine-3-carboxylate (4.51 g, 73%) as a colourless oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | USRE042353E1 |
| 출처 데이터셋 | uspto-grants-2011_05 |
| ORD ID | ord-c68b3b5ec2e34710853692c235db63a0 |
| 출처 메모 | uspto-grants-2011_05 |