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HRID 1395480作成日:2026年10月27日

Ethanol → Ethyl [2-(4-Benzhydrylpiperidino)-2-oxoethoxy]acetate

https://huagongshe.com/reaction/1395480

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物p-Toluenesulfonic acidHCID 6101—
反応物Mcn 4308HCID 196442—
溶媒DichloromethaneHCID 6344—
生成物Ethyl [2-(4-Benzhydrylpiperidino)-2-oxoethoxy]acetateHCID 54306890—

反応手順

To about 50 milliliters of ethanol is added 3.63 grams (10 millimoles) of [2-(4-benzhydrylpiperidino)-2-oxoethoxy]acetic acid (prepared as described in Example V) and 200 milligrams of p-toluenesulfonic acid and the mixture refluxed for about four hours whereupon a reaction takes place with the formation in the reaction mixture of the desired ester product as confirmed by chromatographic analysis. The reaction mixture is subjected to reduced pressure to evaporate the ethanol and to obtain a product residue which is then dissolved in dichloromethane. The dichloromethane solution is first washed with aqueous bicarbonate solution, then dried over potassium carbonate and finally evaporated under reduced pressure to recover an ethyl [2-(4-benzhydrylpiperidino)-2-oxoethoxy]acetate product as residue. The ester product which may be further purified by distillation under reduced pressure has a molecular weight of 391.5.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04203991
出典データセットuspto-grants-1980_05
ORD IDord-21f2aca31b5e42c99d20d0b0d8dcbca7
出典メモuspto-grants-1980_05