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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1269468생성일: 2026년 10월 26일

Pyridine → N-[4-cyano-3-trifluoromethyl-phenyl]-2-hydroxy-3-methanesulfonyloxy-2-methyl-propionamide

https://huagongshe.com/reaction/1269468

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Methanesulfonyl chlorideHCID 31297—
반응물N-[4-cyano-3-(trifluoromethyl)phenyl]-2,3-dihydroxy-2-methylpropanamideHCID 9882395—
용매DichloromethaneHCID 6344—
생성물N-[4-cyano-3-trifluoromethyl-phenyl]-2-hydroxy-3-methanesulfonyloxy-2-methyl-propionamideHCID 12148451—

반응 조건

온도0 °C

반응 단계

A solution of 46 g (0.16 mol) of N-[4-cyano-3-trifluoromethyl-phenyl]-2,3-dihydroxy-2-methyl-propionamide in 1 1 of dichloromethane and 46 ml (0.57 mol) of dry pyridine was cooled to 0° C. and 46 ml (0.59 mol) of methanesulfonyl chloride was added dropwise. The mixture was stirred at 0° C. for 5 h, then washed three times with 500 ml of saturated aqueous sodium hydrogen carbonate, 500 ml of 10% aqueous hydrochloric acid and 500 ml of brine. The organic layer was dried over sodium sulfate and concentrated in vacuum. The residue was crystallized with 200 ml of petroleum ether, which has a boiling range of 40–70° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07199257B1
출처 데이터셋uspto-grants-2007_04
ORD IDord-b35866d175fd4d758effefbba81c681b
출처 메모uspto-grants-2007_04