Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methanesulfonamide → N-(3-bromo-5-fluorobenzyl)methanesulfonamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methanesulfonamide | HCID 72879 | — |
| 반응물 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 반응물 | 3-Bromo-5-fluorobenzaldehyde | HCID 21986246 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 생성물 | N-(3-bromo-5-fluorobenzyl)methanesulfonamide | HCID 47320493 | 99% |
반응 단계
Preparation of 3-bromo-5-fluorobenzaldehyde (XLIX) (2.03 g, 10.0 mmol) in DCE (50 mL) was added methanesulfonamide (1.43 g, 15.0 mmol) and TEA (2.79 mL, 20.0 mmol). The solution was stirred for a few minutes before NaBH(OAc)3 (3.00 g, 14.1 mmol) was added. The reaction was stirred at room temperature overnight. The solvent was removed under vacuum and the residue was partitioned between EtOAc and water. The organic layer was separated, dried over MgSO4 and evaporated under vacuum to give N-(3-bromo-5-fluorobenzyl)methanesulfonamide (L) as a clear oil (2.65 g, 9.39 mmol, 99% yield). ESIMS found C8H9BrFNO2S m/z 282 (M+H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09233104B2 |
| 출처 데이터셋 | uspto-grants-2016_01 |
| ORD ID | ord-f52496bc37724f498712e45f2e2f0a2b |
| 출처 메모 | uspto-grants-2016_01 |