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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1023생성일: 2026년 10월 23일

Acetic Acid → HCID 178418358, 화합물

https://huagongshe.com/ko/reaction/1023

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물1,1-DichloroethaneHCID 6365—
반응물Ethyl orthoformateHCID 31214—
반응물4-PhenylcyclohexanoneHCID 78605—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물3-Bromo-2-ethylpyridin-4-amineHCID 54573798—
촉매Boron trifluoride etherateHCID 8000—
용매EthanolHCID 702—
생성물HCID 178418358HCID 178418358—

반응 조건

온도50 °C

반응 단계

3.48 g (20 mmol) of 4-phenylcyclohexanone in 3.3 ml of ethanol are treated with 3.3 ml of triethyl orthoformate and 2 drops of boron trifluoride etherate and warmed at 50° C. for 30 min. After addition of 2.01 g (10mmol) of 2-ethyl-3-bromo-4-aminopyridine the reaction mixture is heated at 135°-140° C. for 3.5-4 hours with simultaneous removal of the low-boiling components by distillation. It is then cooled, 40 ml of dichloroethane, 3.18 g (15 mmol) of sodium triacetoxyborohydride and 0.57 ml (10 mmol) of glacial acetic acid are added, and it is heated at 50°-60° C. for 3 hours; the reaction mixture is then cooled, saturated aqueous sodium hydrogen carbonate solution is added, the 1,2-dichloroethane is evaporated and the reaction product is extracted from the aqueous phase using ethyl acetate. Purification is carried out by column chromatography. Yield: 1.46 g (41%); RF =0.59 (ethyl acetate)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723450
출처 데이터셋uspto-grants-1998_03
ORD IDord-5d3b4c5598fc43c8868c332153f62858
출처 메모uspto-grants-1998_03