HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646503Generated: October 29, 2026
Diethyl Oxalate → HCID 178473081, compound
https://huagongshe.com/reaction/646503
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 1-(2,4-Bis(benzyloxy)-5-isopropylphenyl)ethanone | HCID 24773361 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178473081 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07705027B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-95f95dd8518b4863a39b393e3386cbf0 |
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| Source note | uspto-grants-2010_04 |
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