Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Formaldehyde → Benzyl 4-cyano-4-(hydroxymethyl)piperidine-1-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Formaldehyde | HCID 712 | — |
| 반응물 | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| 반응물 | Benzyl 4-cyanopiperidine-1-carboxylate | HCID 22028286 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Benzyl 4-cyano-4-(hydroxymethyl)piperidine-1-carboxylate | HCID 66980534 | 41% |
반응 단계
To a mixture of benzyl 4-cyanopiperidine-1-carboxylate (1.0 g, 4.0 mmol, Oakwood) in THF (50 mL) at about −78° C. was added LiHMDS (1.0 M solution in THF, 6.14 mL, 6.14 mmol) dropwise via syringe. The mixture was stirred for about 1 h. Paraformaldehyde (0.25 g, 8.2 mmol) was added in one portion and the mixture was stirred overnight at rt. The mixture was concentrated in vacuo and the residue was purified by preparative TLC (1:1 EtOAc/pet ether) to give benzyl 4-cyano-4-(hydroxymethyl)piperidine-1-carboxylate (0.45 g, 35%): LC/MS (Table 2, Method k) Rt=0.60 min; MS m/z: 274 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08551981B2 |
| 출처 데이터셋 | uspto-grants-2013_10 |
| ORD ID | ord-5c54e5ae32254843bbadc584dacfc6c3 |
| 출처 메모 | uspto-grants-2013_10 |