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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 589453생성일: 2026년 10월 26일

Methanesulfonamide → N-(3-bromo-5-fluorobenzyl)methanesulfonamide

https://huagongshe.com/reaction/589453

반응식

참여 물질

역할이름HCID투입량
반응물MethanesulfonamideHCID 72879—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물3-Bromo-5-fluorobenzaldehydeHCID 21986246—
용매1,2-DichloroethaneHCID 11—
생성물N-(3-bromo-5-fluorobenzyl)methanesulfonamideHCID 4732049399%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09233104B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-f52496bc37724f498712e45f2e2f0a2b
출처 메모uspto-grants-2016_01