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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646503Generated: October 29, 2026

Diethyl Oxalate → HCID 178473081, compound

https://huagongshe.com/reaction/646503

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 1MHCl (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 numberUS07705027B2
Source datasetuspto-grants-2010_04
ORD IDord-95f95dd8518b4863a39b393e3386cbf0
Source noteuspto-grants-2010_04