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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 705186생성일: 2026년 10월 24일

3',5'-Difluoroacetophenone → 2-(3,5-Difluorophenyl)propan-2-ol

https://huagongshe.com/ko/reaction/705186

반응식

참여 물질

역할이름HCID투입량
반응물3',5'-DifluoroacetophenoneHCID 518596—
반응물HCID 178418573HCID 178418573—
용매TetrahydrofuranHCID 8028—
생성물2-(3,5-Difluorophenyl)propan-2-olHCID 57732159—

반응 단계

To a solution of 1-(3,5-difluorophenyl)ethanone (1.0 equiv) in THF (0.2 M) at 0° C. was added methylmagnesium bromide (1.0 M in THF, 1.15 equiv). After stirring for 4 hours the reaction was quenched by addition of NH4Cl(sat), diluted with EtOAc, washed with NaCl(sat), dried over MgSO4, filtered, concentrated and purified by ISCO SiO2 chromatography to yield 2-(3,5-difluorophenyl)propan-2-ol. To a solution of 2-(3,5-difluorophenyl)propan-2-ol in CH2Cl2 (0.1 M) at 0° C. was added 2,6 lutidine (6 equiv.) and than triisopropylsilyl trifluoromethanesulfonate (3.0 equiv.). After stirring for 3 hours at 0° C. and six hours at rt the solution was partitioned between EtOAc and NaHCO3(sat), separated, washed with NaCl(sat), dried over MgSO4, filtered, concentrated and purified by ISCO SiO2 chromatography to yield (2-(3,5-difluorophenyl)propan-2-yloxy)triisopropylsilane. (400 MHz, <cdcl3>) δ ppm 1.05-1.08 (m, 21 H) 1.57 (s, 6 H) 6.63 (s, 1 H) 7.00 (dd, J=9.39, 2.35 Hz, 2 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09173883B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-044e148c4ab54996ba08bcc06ca37a6f
출처 메모uspto-grants-2015_11