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HRID 638634생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/638634

반응식

참여 물질

역할이름HCID투입량
반응물AcetanilideHCID 904—
반응물Potassium CarbonateHCID 11430—
반응물3-Bromo-4-fluorobenzyl 2,2-dimethyl-2-(4-ethoxyphenyl)ethyl etherHCID 13488190—
용매DimethylformamideHCID 6228—
생성물3-Anilino-4-fluorobenzyl 2,2-dimethyl-2-(4-ethoxyphenyl)ethyl etherHCID 13363848—

반응 조건

온도140 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04562213
출처 데이터셋uspto-grants-1985_12
ORD IDord-9e80d37ee8754ea2978e2c48634843e2
출처 메모uspto-grants-1985_12