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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1395480생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1395480

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물p-Toluenesulfonic acidHCID 6101—
반응물Mcn 4308HCID 196442—
용매DichloromethaneHCID 6344—
생성물Ethyl [2-(4-Benzhydrylpiperidino)-2-oxoethoxy]acetateHCID 54306890—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04203991
출처 데이터셋uspto-grants-1980_05
ORD IDord-21f2aca31b5e42c99d20d0b0d8dcbca7
출처 메모uspto-grants-1980_05