Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Propanal → tert-Butyl 4-(3-hydroxy-1-oxopent-1-yl)-4-methoxypiperidine-1-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Propanal | HCID 527 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Tert-butyl 4-acetyl-4-methoxypiperidine-1-carboxylate | HCID 21983927 | — |
| 반응물 | Lithium diisopropylamine | HCID 45051747 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | tert-Butyl 4-(3-hydroxy-1-oxopent-1-yl)-4-methoxypiperidine-1-carboxylate | HCID 21984004 | 55.9% |
반응 단계
To a solution of tert-butyl 4-acetyl-4-methoxypiperidine-1-carboxylate (0.589 g, 2.29 mmol) from Step A in tetrahydrofuran (20 mL) at −78° C. was added lithium diisopropylamine (0.650 mL, 0.974 mmol) followed by propionaldehyde (0.266 g, 0.330 mL, 4.58 mmol). After 5 min, the reaction mixture was poured into saturated ammonium chloride, and extracted three times with diethyl ether. The organic layers were combined, washed with saturated sodium chloride solution, dried over sodium sulfite, filtered, and concentrated. The residue was purified by flash chromatography eluting with 40% ethyl acetate/hexanes to afford the title compound (0.404 g). MS/EI (acetonitrile/water): m/z 216.1 (M+1−BOC) retention time=2.69 min.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07091211B2 |
| 출처 데이터셋 | uspto-grants-2006_08 |
| ORD ID | ord-b89820f3efd14138aa3a6cb136df92cc |
| 출처 메모 | uspto-grants-2006_08 |