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HRID 747678作成日:2026年10月26日

Benzocaine → Ethyl 4-(piperidin-1-yl)benzoate

https://huagongshe.com/reaction/747678

反応式

関与物質

役割名称HCID仕込み量
反応物BenzocaineHCID 2337—
反応物1,5-DibromopentaneHCID 8100—
反応物DiisopropylethylamineHCID 81531—
溶媒BenzeneHCID 241—
溶媒WaterHCID 962—
生成物Ethyl 4-(piperidin-1-yl)benzoateHCID 13813852—

反応手順

2.16 g (13.1 mmol) of ethyl 4-aminobenzoate was dissolved in 20 ml of benzene. 2.97 g (13.0 mmol) of 1,5-dibromopentane and 4.53 ml (26.0 mmol) of diisopropylethylamine were added to the solution, and they were heated under reflux for 48 hours. The reaction liquid was diluted with water. After the extraction with ethyl acetate, the organic layer was washed with water and then with saturated aqueous NaCl solution, and dried over anhydrous magnesium sulfate. The solvent was evaporated to obtain the crude title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07396844B1
出典データセットuspto-grants-2008_07
ORD IDord-ad3bbc83df2049d0ab063b65240d4ace
出典メモuspto-grants-2008_07