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HRID 638634作成日:2026年10月27日

Acetanilide → 3-Anilino-4-fluorobenzyl 2,2-dimethyl-2-(4-ethoxyphenyl)ethyl ether

https://huagongshe.com/reaction/638634

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3-Bromo-4-fluorobenzyl 2,2-dimethyl-2-(4-ethoxyphenyl)ethyl etherHCID 13488190—
溶媒DimethylformamideHCID 6228—
生成物3-Anilino-4-fluorobenzyl 2,2-dimethyl-2-(4-ethoxyphenyl)ethyl etherHCID 13363848—

反応条件

温度140 °C

反応手順

2.37 Grams of 3-bromo-4-fluorobenzyl 2,2-dimethyl-2-(4-ethoxyphenyl)ethyl ether, 0.95 g of potassium carbonate, 1.01 g of acetanilide, 10 ml of dimethylformamide and 250 mg of cuprous chloride were mixed and stirred at 140° C. for 40 hours in a nitrogen stream. The reaction mixture was poured into ice water and extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous sodium chloride liquor, and after removing the solvent by evaporation, the residual oil was dissolved in a 20% ethanol solution of potassium hydroxide (2 times by mole) and refluxed for 30 minutes. The reaction solution was then poured into ice water and extracted with ether. The ether layer was washed with an aqueous sodium chloride liquor and dried over anhydrous magnesium sulfate, and the solvent was removed by evaporation. The residual oil was separation-purified by column chromatography on silica gel to obtain 1.05 g of 3-anilino-4-fluorobenzyl 2,2-dimethyl-2-(4-ethoxyphenyl)ethyl ether.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04562213
出典データセットuspto-grants-1985_12
ORD IDord-9e80d37ee8754ea2978e2c48634843e2
出典メモuspto-grants-1985_12