Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097289Generated: October 31, 2026

Diethyl Oxalate → HCID 178473081, compound

https://huagongshe.com/reaction/2097289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl OxalateHCID 7268—
ReactantSodium ethoxideHCID 2723922—
ReactantSodiumHCID 5360545—
Reactant1-(2,4-Bis(benzyloxy)-5-isopropylphenyl)ethanoneHCID 24773361—
SolventEthanolHCID 702—
ProductHCID 178473081HCID 178473081—

Reaction Steps

Sodium (2.8 eq) was added to ethanol under nitrogen at room temperature and stirred for 25 minutes to generate sodium ethoxide. 1-(2,4-Bis-benzyloxy-5-isopropyl-phenyl)-ethanone (1 eq) was dissolved in further ethanol and added to the sodium ethoxide solution. Diethyl oxalate (1.64 eq) was added and the reaction mixture heated to reflux for 4 hours. The mixture was allowed to cool to room temperature and enough 1 MHCl (aq) was added to acidify the reaction mixture, which was then concentrated in vacuo. The resulting gum was partitioned between dichloromethane and brine, and the organic phase was dried over MgSO4, filtered and evaporated in vacuo to give 4-(2,4-Bis-benzyloxy-5-isopropyl-phenyl)-2-hydroxy-4-oxo-but-2-enoic acid ethyl ester as a yellow gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450310B2
Source datasetuspto-grants-2013_05
ORD IDord-346d0c00f5014fd990b2c1ff9c54eb13
Source noteuspto-grants-2013_05