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HRID 647328作成日:2026年10月25日

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

https://huagongshe.com/reaction/647328

反応式

関与物質

役割名称HCID仕込み量
反応物4-Piperidinecarboxylic acidHCID 3773—
反応物1,1-DichloroethaneHCID 6365—
反応物1,4-DimethoxybenzeneHCID 9016—
反応物Thionyl ChlorideHCID 24386—
反応物Aluminum(III) ChlorideHCID 6451240—
生成物1-Acetyl-4-(2-hydroxy-5-methoxybenzoyl)piperidineHCID 13076384—

反応手順

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 giave 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°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04408054
出典データセットuspto-grants-1983_10
ORD IDord-4c058aa86d314b4a8a26d4f8219211c8
出典メモuspto-grants-1983_10