Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371972Generated: October 30, 2026

Oxalyl chloride → HCID 53863562, compound

https://huagongshe.com/reaction/2371972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 14557730HCID 14557730—
SolventDichloromethaneHCID 6344—
ProductHCID 53863562HCID 53863562—

Reaction Steps

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05096925
Source datasetuspto-grants-1992_03
ORD IDord-1a6cd78087844d4ba50030307119836c
Source noteuspto-grants-1992_03