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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 223557생성일: 2026년 10월 25일

4-Piperidinecarboxylic acid → 1-Acetyl-4-(2-hydroxy-5-methoxybenzoyl)piperidine

https://huagongshe.com/reaction/223557

반응식

참여 물질

역할이름HCID투입량
반응물4-Piperidinecarboxylic acidHCID 3773—
반응물1,1-DichloroethaneHCID 6365—
반응물1,4-DimethoxybenzeneHCID 9016—
반응물Thionyl ChlorideHCID 24386—
반응물Aluminum(III) ChlorideHCID 6451240—
생성물1-Acetyl-4-(2-hydroxy-5-methoxybenzoyl)piperidineHCID 13076384—

반응 단계

To a stirred mixture of 60.0 g of isonipecotic acid and 290 ml of 1,2-dichloromethane, at 40°, was added dropwise, 27 ml of thionyl chloride, dissolved in 27 ml of dichloroethane. After 50% of the thionyl chloride had been added, the temperature was raised to 65°. After complete addition of the thionyl chloride, the reaction mixture was stirred at 65° for 1 hr. The reaction mixture was cooled to 20° and 48.6 g of 1,4-dimethoxybenzene was added, followed by the slow addition of 93.6 g of aluminum chloride. The solution was heated under reflux for 4 hrs, the dichloroethane was decanted from the insoluble complex, and concentrated hydrochloric acid was added. The acid hydrolysate was added to the dichloroethane solution and the mixture was extracted three times with chloroform. The organic extract was washed with water, dried over anhydrous magnesium sulfate and the solvent was removed in vacuo to give an oil. The oil was scratched with a glass rod until crystallization was effected. The solid was collected to yield 87.0 g of product. Recrystallization twice from isopropyl ether gave an analytically pure product, mp, 93°-94°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04355037
출처 데이터셋uspto-grants-1982_10
ORD IDord-a008fed1622a424897178425804476a0
출처 메모uspto-grants-1982_10