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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280976Generated: October 28, 2026

Diethyl Malonate → Ethyl 5-(1-benzyloxycarbonyl-4-piperidyl)-2-ethoxycarbonylvalerate

https://huagongshe.com/reaction/280976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
ReactantSodiumHCID 5360545—
Reactant3-(1-Benzyloxycarbonyl-4-piperidyl)propyl p-toluenesulfonateHCID 13652731—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductEthyl 5-(1-benzyloxycarbonyl-4-piperidyl)-2-ethoxycarbonylvalerateHCID 20143730—

Reaction Steps

To a solution of sodium (5.8 g) in ethanol (300 ml) are added diethyl malonate (40 g) and 3-(1-benzyloxycarbonyl-4-piperidyl)propyl p-toluenesulfonate (90.5 g). The resulting mixture is refluxed for 2 hours with stirring, cooled, diluted with water (1 l) and extracted with ethyl acetate (500 ml). The extract is dried over magnesium sulfate and evaporated in vacuo to give ethyl 5-(1-benzyloxycarbonyl-4-piperidyl)-2-ethoxycarbonylvalerate as an oil. To the stirred solution of this oil in ethanol (200 ml) is added dropwise a solution of sodium hydroxide (34 g) in water (200 ml). After the addition is complete, the mixture is diluted with water (300 ml) and extracted with a mixture of ether and petroleum ether (1:1, 300 ml). The aqueous layer is acidified with concentrated hydrochloric acid and extracted with ethyl acetate (500 ml). The extract is washed with water, dried over anhydrous magnesium sulfate and evaporated in vacuo to yield 5-(1-benzyloxycarbonyl-4-piperidyl)-2-carboxyvaleric acid as an oil. This oil is heated at 160°-170° C. for 45 minutes with stirring to give 5-(1-benzyloxycarbonyl-4-piperidyl)valeric acid (50 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04591458
Source datasetuspto-grants-1986_05
ORD IDord-350612330c0349829e41bd256aa8b8fc
Source noteuspto-grants-1986_05