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HRID 218504생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/218504

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 조건

온도80 °C

반응 단계

28.5 g (228 mol) of 3-methoxypyridin-2(1H)-one are dissolved in 850 ml of dimethyl sulfoxide and admixed at RT with 31 g (273 mmol) of potassium tert-butoxide. The suspension is stirred at RT for 30 min, before 35 g (228 mmol) of 1-fluoro-2-methyl-4-nitrobenzene are added, and the reaction solution is heated to 80° C. for 20 h. The mixture is then cautiously diluted with 1 l of water and brought to pH 1-2 with 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 sulfate, filtered and concentrated under reduced pressure. The resulting solid is washed with a little tert-butyl methyl ether, filtered off and dried under reduced pressure. This affords 42.8 g (72% of theory) of the desired compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198267B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-ff66636a79984f4390ae566357b10ac0
출처 메모uspto-grants-2012_06