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HRID 1597484作成日:2026年10月27日

Ethyl trifluoroacetate → Butane-1,3-dione, 4,4,4-trifluoro-1-(4-imidazol-1-ylphenyl)-

https://huagongshe.com/reaction/1597484

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl trifluoroacetateHCID 9794—
反応物HexamethyldisilazaneHCID 13838—
反応物1-(4-(1H-Imidazol-1-yl)phenyl)ethanoneHCID 82316—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物Butane-1,3-dione, 4,4,4-trifluoro-1-(4-imidazol-1-ylphenyl)-HCID 6426099—

反応条件

温度-78 °C

反応手順

To a THF (5 mL) solution of 1,1,1,3,3,3-hexamethyldisilazane (0.178 g, 1.1 mmol) was added n-butyl lithum (1.6 M solution in hexane, 0.72 mL, 1.2 mmol) at 0° C. under nitrogen, and the mixture was stirred for 30 minutes, and cooled to −78° C. 4-(1-Imidazolyl)acetophenone (prepared according the method of M. A. Khan et. al., J. Chem. Soc. C., 1970, 85., 0.186 g, 1.0 mmol) was added to the mixture, and residue was stirred for 1 hour. Ethyl trifluoroacetate (0.17 g, 1.2 mmol) was added to the reaction mixture, the residure was warm to room temperature. The reaction mixture was poured into ice water and the whole was extracted with ethyl acetate (30 mL×2). The organic layer was washed with brine, dried over Na2SO4, and concentrated in vacuo. The resulting solid was washed with small amount of ethyl acetate to give the title compound (0.163 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06294558B1
出典データセットuspto-grants-2001_09
ORD IDord-dd99a2f70be241dfb12ab52cfb0b765d
出典メモuspto-grants-2001_09