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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649397Generated: October 29, 2026

Diethyl Malonate → 5-(1-Benzyloxycarbonyl-4-piperidyl)-2-carboxyvaleric acid

https://huagongshe.com/reaction/649397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
ReactantSodium HydroxideHCID 14798—
ReactantSodiumHCID 5360545—
Reactant3-(1-Benzyloxycarbonyl-4-piperidyl)propyl p-toluenesulfonateHCID 13652731—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product5-(1-Benzyloxycarbonyl-4-piperidyl)-2-carboxyvaleric acidHCID 20143680—

Reaction Steps

In 300 ml of ethanol is dissolved 5.8 g of sodium, and 40 g of diethyl malonate is added to the solution, followed by stirring. 3-(1-Benzyloxycarbonyl-4-piperidyl)propyl p-toluenesulfonate (90.5 g) is added to this mixture followed by refluxing with stirring for 2 hours. After cooling, 1 l of water is added to the reaction solution, which is then extracted with 500 ml of ethyl acetate. The extract is dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give ethyl 5-(1-benzyloxycarbonyl-4-piperidyl)-2-ethoxycarbonylvalearate as an oily material. This product is dissolved in 200 ml of ethanol, and a solution of 34 g of sodium hydroxide in 200 ml of water is added dropwise to the solution with stirring. After the addition is completed, 300 ml of water is added to the reaction solution, which is then extracted with a mixture of ether and petroleum ether (1:1, 300 ml). The aqueous layer is made acidic with conc. hydrochloric acid, followed by extraction with 500 ml of ethyl acetate. The extract is washed with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 5-(1-benzyloxycarbonyl-4-piperidyl)-2-carboxyvaleric acid as an oily material. This product is heated at 160° to 170° C. with stirring for 45 minutes to give 50 g of 5-(1-benzyloxycarbonyl-4-piperidyl)valeric acid as an oily material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04739066
Source datasetuspto-grants-1988_04
ORD IDord-b48cc7112aa649f8b7e46e5602a2a926
Source noteuspto-grants-1988_04