HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395480Generated: October 26, 2026
Ethanol → Ethyl [2-(4-Benzhydrylpiperidino)-2-oxoethoxy]acetate
https://huagongshe.com/reaction/1395480
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Mcn 4308 | HCID 196442 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl [2-(4-Benzhydrylpiperidino)-2-oxoethoxy]acetate | HCID 54306890 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04203991 |
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| Source dataset | uspto-grants-1980_05 |
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| ORD ID | ord-21f2aca31b5e42c99d20d0b0d8dcbca7 |
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| Source note | uspto-grants-1980_05 |
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