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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 238932생성일: 2026년 10월 25일

Hydrochloric Acid → N-(4-Acetyl-2-fluorophenyl)methanesulfonamide

https://huagongshe.com/reaction/238932

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Butyl vinyl etherHCID 8108—
반응물thallium(I) acetateHCID 11247—
반응물N-(2-Fluoro-4-iodophenyl)methanesulfonamideHCID 19785608—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물N-(4-Acetyl-2-fluorophenyl)methanesulfonamideHCID 58755745—

반응 조건

온도95 °C

반응 단계

A mixture of N-(2-Fluoro-4-iodophenyl)methanesulfonamide (13-3, 5 mmol) and palladium(II)acetate (0.15 nM, 0.034 g), 1,3-bisdiphenyl phosphinoprophan (0.3 mM, 0.124 g), thallium(I)acetate (5.5 mM, 1.450 g) and butylvinyl ether (10 mM, 1.3 mL) in DMF (10 mL) was heated at 95° C. for 19 h. The reaction mixture was cooled to room temperature, diluted with THF, treated with 10% HCl (10 mL) and stirred at room temperature. A mixture was diluted with EtOAc, washed with ammonium chloride solution three times and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel using EtOAc:hexanes as eluant to 3′-Fluoro-4′-(methylsulfonylamino)acetophenone (13-6, LJO-363).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642657B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-1e154d2223aa4f1f859ba08d87aad887
출처 메모uspto-grants-2014_02