Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triphenylphosphine → tert-butyl (R)-3-(2-ethoxyphenoxy)piperidine-1-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | 2-Ethoxyphenol | HCID 66755 | — |
| 반응물 | tert-butyl (3S)-3-hydroxypiperidine-1-carboxylate | HCID 1514399 | — |
| 반응물 | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | tert-butyl (R)-3-(2-ethoxyphenoxy)piperidine-1-carboxylate | HCID 131737068 | 45.9% |
반응 단계
To a solution of 2-ethoxyphenol (13.72 g, 99 mmol), tert-butyl (S)-3-hydroxypiperidine-1-carboxylate (20 g, 99 mmol), and triphenylphosphine (29 g, 111 mmol) in toluene (150 mL) at 20-25° C. was added a solution of DIAD (20 mL, 104 mmol) in toluene (50 mL) over 2 hours. After 2 hours, the reaction mixture was filtered and washed with diethyl ether (300 mL). The filtrate was washed with 3N NaOH (150 mL), dried over Na2SO4, and concentrated. The crude residue was purified via column chromatography to afford tert-butyl (R)-3-(2-ethoxyphenoxy)piperidine-1-carboxylate (14.6 g, 45%). MS (ES+) 222.2 (M-100+H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09440949B2 |
| 출처 데이터셋 | uspto-grants-2016_09 |
| ORD ID | ord-84c2c17968264ec79a61826a50901a96 |
| 출처 메모 | uspto-grants-2016_09 |