戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 705186作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物3',5'-DifluoroacetophenoneHCID 518596—
反応物HCID 178418573HCID 178418573—
溶媒TetrahydrofuranHCID 8028—
生成物2-(3,5-Difluorophenyl)propan-2-olHCID 57732159—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09173883B2
出典データセットuspto-grants-2015_11
ORD IDord-044e148c4ab54996ba08bcc06ca37a6f
出典メモuspto-grants-2015_11