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HRID 414503作成日:2026年10月25日

Acetanilide → 1,1-Difluoro-2,2-dimethyl-3-[3-(N-phenyl-N-acetylamino)-4-fluorobenzyloxy]propane

https://huagongshe.com/reaction/414503

反応式

関与物質

役割名称HCID仕込み量
反応物AcetanilideHCID 904—
反応物Potassium CarbonateHCID 11430—
反応物Ethanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]-HCID 112414—
反応物1,1-Difluoro-2,2-dimethyl-3-(3-bromo-4-fluorobenzyloxy)propaneHCID 21281078—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物1,1-Difluoro-2,2-dimethyl-3-[3-(N-phenyl-N-acetylamino)-4-fluorobenzyloxy]propaneHCID 2128108938.6%

反応手順

A mixture of 1,1-difluoro-2,2-dimethyl-3-(3-bromo-4-fluorobenzyloxy)propane (1.5 g), acetanilide (0.716 g), cuprous chloride (0.1 g); potassium carbonate (0.67 g), dry N,N-dimethylformamide (10 cm3) and tri[2-(2-methoxyethoxy)ethyl]amine (catalytic quantity) was heated at 158° C. for 4 days under an atmosphere of nitrogen; the mixture was then stood at the ambient temperature for 1 week. The combined organic extracts were washed with water and brine and dried over anhydrous magnesium sulphate. Evaporation of the solvent under reduced pressure gave a dark oil which was subjected to flash column chromatography on a silica gel support, eluting firstly with petroleum ether (boiling range 40°-6° C.) containing 2% by volume ethyl acetate (to give starting materials and a small amount of the deacylated product) and secondly with petroleum ether (boiling range 40°-60° C.) containing 50% by volume ethyl acetate, to give the title compound as a dark oil (0.68 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04792563
出典データセットuspto-grants-1988_12
ORD IDord-f709d9e00203454e8dcc3eb8d1b0d612
出典メモuspto-grants-1988_12