돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 391744생성일: 2026년 10월 24일

Hydrochloric Acid → 3-Methoxy-1-(2-methyl-4-nitrophenyl)pyridin-2(1H)-one

https://huagongshe.com/ko/reaction/391744

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Benzene, 1-fluoro-2-methyl-4-nitro-HCID 68001—
반응물3-Methoxy-2-pyridoneHCID 88731—
반응물Potassium tert-butoxideHCID 23665647—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물3-Methoxy-1-(2-methyl-4-nitrophenyl)pyridin-2(1H)-oneHCID 59410165—

반응 단계

28.5 g (228 mol) of 3-methoxypyridin-2(1H)-one are dissolved in 850 ml of dimethyl sulphoxide, and 31 g (273 mmol) of potassium tert-butoxide are added at RT. The suspension is stirred at RT for 30 min, and 35 g (228 mmol) of 1-fluoro-2-methyl-4-nitrobenzene are then added, and the reaction solution is heated at 80° C. for 20 h. The solution is then carefully diluted with 1 l of water and adjusted to pH 1-2 using 1N hydrochloric acid. The solution is extracted repeatedly with dichloromethane. The combined organic extracts are washed with water and saturated sodium chloride solution, dried over sodium sulphate, filtered and evaporated under reduced pressure. The solid obtained is washed with a little tert-butyl methyl ether, filtered off and dried under reduced pressure. This gives 42.8 g (72% of theory) of the desired compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08383822B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-d9469ce27326464cb179eeadf6274cd8
출처 메모uspto-grants-2013_02