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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1583583생성일: 2026년 10월 26일

Dimethylformamide → Ethyl 3-(2-fluoroethoxy)benzoate

https://huagongshe.com/reaction/1583583

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물1-Chloro-2-fluoroethaneHCID 12983—
반응물Ethyl 3-hydroxybenzoateHCID 24522—
용매WaterHCID 962—
생성물Ethyl 3-(2-fluoroethoxy)benzoateHCID 1505863385.1%

반응 단계

Thirty grams of ethyl 3-hydroxybenzoate, 14.9 g of 1-fluoro-2-chloroethane and 37.4 g of anhydrous potassium carbonate were added to 130 ml of dimethylformamide. With stirring, the reaction was carried out at 120° C. for 4 hours. The reaction mixture was cooled to room temperature, poured into water, and extracted with toluene. The toluene layer was washed with water, and dried over anhydrous sodium sulfate. Toluene was evaporated under reduced pressure to give 32.6 g of crude ethyl 3-(2-fluoroethoxy)benzoate. The resulting crude ethyl 3-(2-fluoroethoxy)benzoate (32.6 g) was added at 40° to 45° C. to a solution of 6.0 g of lithium aluminum hydride in 200 ml of dry tetrahydrofuran, and the mixture was heated under reflux for 2 hours. After the reaction, the reaction mixture was cooled to room temperature. Ethanol and water in this order were added to the mixture to decompose the unreacted lithium aluminum hydride. Water was then added, and the mixture was extracted with toluene. The toluene layer was washed with water, and dried over anhydrous sodium sulfate. Toluene was removed to give 26.0 g of crude 3-(2-fluoroethoxy)benzyl alcohol This compound was chlorinated to give 30.0 g of 3-(2-fluoroethoxy)benzyl chloride.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04552894
출처 데이터셋uspto-grants-1985_11
ORD IDord-3f744ca3762f42798fc66784e4344780
출처 메모uspto-grants-1985_11