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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 35885생성일: 2026년 10월 24일

Methyl trifluoromethyl ketone → 1-(4-Phenylsulfonylphenyl)-3-hydroxy-3-methyl-4,4,4-trifluorobut-1-yne

https://huagongshe.com/ko/reaction/35885

반응식

참여 물질

역할이름HCID투입량
반응물Methyl trifluoromethyl ketoneHCID 9871—
반응물4-PhenylsulfonylphenylethyneHCID 19939320—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1-(4-Phenylsulfonylphenyl)-3-hydroxy-3-methyl-4,4,4-trifluorobut-1-yneHCID 1993930375.3%

반응 단계

To a cooled (-78° C.) solution of 4-phenylsulfonylphenylethyne (66 mg, 0.27 mmol) in freshly distilled tetrahydrofuran (2.5 mL) was added n-BuLi (109 mL, 2.5M solution in hexanes, 0.27 mmol). The solution was stirred for 10 minutes at -78° C. at which time 1,1,1-trifluoroacetone (272 mL, 1.0M solution in tetrahydrofuran, 0.27 mmol) was added. The reaction mixture was kept at -78° C. for five minutes before quenching with 2N HCl . Diethyl ether was added, and the aqueous layer extracted further with diethyl ether. The combined organic layers were dried, evaporated and the product purified by chromatography, with ethyl acetate:hexanes as eluent (1:4) to yield the title butyne as a white solid (72 mg, 75%); mp 94.8°-95.3° C.; 250 MHz NMR (CDCl3): 1.72 (s,3, CH3), 3.08 (s,1, OH), 7.48-7.60 (m,5, Ar), 7.87-7.94 (m,4, Ar); MS: m/z=355(M+ 1). Analysis for C17H13F3O3S: Calculated: C, 57.62; H, 3.70; Found: C, 57.46; H, 3.65.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05411973
출처 데이터셋uspto-grants-1995_05
ORD IDord-15e03f81b99f4241a3b39f8284c311e9
출처 메모uspto-grants-1995_05