돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 859673생성일: 2026년 10월 25일

Methanesulfonyl chloride → N-(4-bromo-2-ethylphenyl)methanesulfonamide

https://huagongshe.com/reaction/859673

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonyl chlorideHCID 31297—
반응물4-Bromo-2-ethylanilineHCID 2801283—
용매PyridineHCID 1049—
용매Ethyl AcetateHCID 8857—
생성물N-(4-bromo-2-ethylphenyl)methanesulfonamideHCID 646915281%

반응 단계

4-Bromo-2-ethyl-aniline (2 mL, 14 mmol) dissolved in anhydrous pyridine (35 mL) at toom temperature was treated with methylsulfonyl chloride (1.3 mL, 16.8 mmol). The reaction was stirred at that temperature for 15 hours before it was diluted with EtOAc. The mixture was washed with H2O, brine and dried over MgSO4. The solvent was removed in vacuo and the residue was purified with flash chromatography (SiO2, 5–30% EtOAc in hexanes) to afford the desired product (3.1 g, 81% yield). 1H NMR (300 MHz, CDCl3): δ 1.25 (t, J=7.5 Hz, 3 H), 2.61–2.68 (m, 2 H), 3.02 (s, 3 H), 6.36 (s, 1 H), 7.36–7.39 (m, 3 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07151105B2
출처 데이터셋uspto-grants-2006_12
ORD IDord-389a00c858154614be5cd1adf398aead
출처 메모uspto-grants-2006_12