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HRID 57461생성일: 2026년 10월 23일

tert-Butylsulfinamide, (R)-(+)- → (NE,R)-N-[[4-(1,1-difluoroethyl)-2-fluorophenyl]methylidene]-2-methylpropane-2-sulfinamide

https://huagongshe.com/ko/reaction/57461

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참여 물질

역할이름HCID투입량
반응물tert-Butylsulfinamide, (R)-(+)-HCID 10964479—
반응물4-(1,1-Difluoroethyl)-2-fluorobenzaldehydeHCID 90414785—
촉매Copper SulfateHCID 24462—
용매1,2-DichloroethaneHCID 11—
생성물(NE,R)-N-[[4-(1,1-difluoroethyl)-2-fluorophenyl]methylidene]-2-methylpropane-2-sulfinamideHCID 9041419646.3%

반응 조건

온도55 °C

반응 단계

To a mixture of 4-(1,1-difluoroethyl)-2-fluorobenzaldehyde (693 mg, from Step 4) and (R)-2-methylpropane-2-sulfinamide (513 mg, 4.24 mmol) in DCE (12.9 mL) was added copper(II) sulfate (882 mg, 5.52 mmol). The reaction mixture was placed in a pre-heated oil bath (55° C.) and heated for ˜2 d. The mixture was allowed to cool to room temperature, filtered through a pad of celite and rinsed with DCE. The combined filtrates were concentrated under reduced pressure. The residue was purified by column chromatography [SiO2, 24 g, heptane/ethyl acetate] providing (R,E)-N-(4-(1,1-difluoroethyl)-2-fluorobenzylidene)-2-methylpropane-2-sulfinamide (497 mg) as a yellow oil. LCMS m/z 292.1 (M+H)+, Rt 0.97 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434719B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-574f6ecd80b143f8b47b401ea8b0dd74
출처 메모uspto-grants-2016_09