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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55550생성일: 2026년 10월 24일

Acetic Acid → 2-Isopropylthio-3-(cyclohexanon-2-yloxy)-pyridine

https://huagongshe.com/ko/reaction/55550

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Potassium CarbonateHCID 11430—
반응물2-ChlorocyclohexanoneHCID 13203—
반응물3-Pyridinol, 2-[(1-methylethyl)thio]-HCID 19957932—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물2-Isopropylthio-3-(cyclohexanon-2-yloxy)-pyridineHCID 5701835572.7%

반응 단계

7.29 g of 2-chlorocyclohexanone are added at room temperature to a mixture of 8.4 g of 2-isopropylthio-3-hydroxypyridine and 7.6 g of potassium carbonate in 120 ml of dimethylformamide, and the mixture is stirred for one hour at 45°-50° C. After the addition of 1.46 g of 2-chlorocyclohexanone and 1.52 g of potassium carbonate and after 2 hours of a further analogous addition of 0.73 g of 2-chlorocyclohexanone and 0.76 g of potassium carbonate, the suspension is stirred for a further 3.5 hours at 45°-50° C. The resulting reaction solution is poured onto a mixture consisting of 200 ml of ice-water, 50 ml of 2N acetic acid and 100 ml of ethyl acetate, washed three times with 300 ml of ethyl acetate and 100 ml of saturated sodium chloride solution each time, dried over sodium sulfate and concentrated by evaporation. The residue is triturated with petroleum ether and filtered. 9.57 g of the desired ketone having a melting point of 106°-110° C. are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05625071
출처 데이터셋uspto-grants-1997_04
ORD IDord-917b3d08128a40d7a7314a146b67dcc5
출처 메모uspto-grants-1997_04