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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374316Generated: October 25, 2026

Oxalyl chloride → 4-ethoxycarbonyl-(S,S)-2,4-dibenzylbutyryl chloride

https://huagongshe.com/reaction/374316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant4-ethoxycarbonyl(S,S)-2,4-dibenzylbutyric acidHCID 14557731—
SolventDichloromethaneHCID 6344—
Product4-ethoxycarbonyl-(S,S)-2,4-dibenzylbutyryl chlorideHCID 14997130—

Reaction Steps

The starting material is prepared as follows: 4.0 g of (S,S)-2,4-dibenzylglutaric anhydride is refluxed in 40 ml of ethanol:toluene (3:2) overnight. The reaction mixture is concentrated to yield 4-ethoxycarbonyl-(S,S)-2,4-dibenzylbutyric acid as an oil. Oxalyl chloride (3.5 ml) is added to the solution of 4.5 g of 4-ethoxycarbonyl-(S,S)-2,4-dibenzylbutyric acid in 10 ml of methylene chloride. The mixture is stirred at room temperature overnight and evaporated to yield 4-ethoxycarbonyl-(S,S)-2,4-dibenzylbutyryl chloride, which is used as such without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05166212
Source datasetuspto-grants-1992_11
ORD IDord-df78d6aa47bc4d3abd6fb032629fa0a4
Source noteuspto-grants-1992_11