Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
3-Methoxybenzylamine → HCID 57754052, 화합물
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 3-Methoxybenzylamine | HCID 21156 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Trifluoromethanesulfonic acid, lithium salt | HCID 3664839 | — |
| 반응물 | (1R,2S)-[2-(3,4-difluoro-phenyl)-1-oxiranyl-ethyl]-carbamic acid tert-butyl ester | HCID 86616462 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | HCID 57754052 | HCID 57754052 | — |
반응 단계
A solution of (1R,2S)-[2-(3,4-difluoro-phenyl)-1-oxiranyl-ethyl]-carbamic acid tert-butyl ester (0.03 g, 0.1 mmol) in acetonitrile (1 mL) was treated with lithium triflate (0.032 g, 0.2 mmol) and stirred at ambient temperature for 20 minutes. Then 3-methoxybenzylamine (0.016 mL, 0.12 mmol) was added to the reaction neat in one portion. The reaction was stirred at ambient temperature for 14 hours. The reaction was poured into saturated ammonium chloride solution (5 mL), extracted with ethyl acetate, the organic phase separated, dried (MgSO4) and the solvent removed at reduced pressure. The product was obtained as an oil and used without further purification (0.041 g, 94%). MS: 437 (M+H, 100%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07557137B2 |
| 출처 데이터셋 | uspto-grants-2009_07 |
| ORD ID | ord-102b0fd138274c048ebe5de232edecef |
| 출처 메모 | uspto-grants-2009_07 |