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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 858578생성일: 2026년 10월 27일

Pyridine → N-[(1R)-1-(4-bromophenyl)ethyl]methanesulfonamide

https://huagongshe.com/reaction/858578

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Methanesulfonyl chlorideHCID 31297—
반응물(R)-4-bromo-alpha-methylbenzylamineHCID 853000—
용매DichloromethaneHCID 6344—
생성물N-[(1R)-1-(4-bromophenyl)ethyl]methanesulfonamideHCID 2856045858%

반응 조건

온도25 °C

반응 단계

To a stirred solution of (R)-(+)-1-(4-bromophenyl)ethylamine (0.5 g, 2.49 mmol), in anhydrous CH2Cl2 (5 mL) under argon were added methane sulfonyl chloride (0.23 mL, 2.99 mmol) and Pyridine (0.30 mL, 3.73 mmol). The resulting solution was stirred at 25° C. for 3 hrs. The reaction mixture was quenched with 1 N HCl and extracted with EtOAc (30 mL). The organic phase was washed with brine (50 mL), dried over Na2SO4 and evaporated. The residue was purified by flash column chromatography (80% EtOAc in hexanes) to give the product (0.40 g, 58%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07148226B2
출처 데이터셋uspto-grants-2006_12
ORD IDord-efb1bf49ff7544b984f4837cf26f0507
출처 메모uspto-grants-2006_12