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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437615Generated: November 2, 2026

Diethyl Oxalate → HCID 359722, compound

https://huagongshe.com/reaction/1437615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl OxalateHCID 7268—
ReactantSodium hydrideHCID 24758—
Reactant4-Chlorobenzyl cyanideHCID 241582—
SolventTetrahydrofuranHCID 8028—
ProductHCID 359722HCID 35972294%

Reaction Conditions

Temperature37.5 °C

Reaction Steps

About 20% of a solution of p-chlorobenzyl cyanide (0.75 g, 4.94 mmol) and diethyl oxalate (0.87 mL, 6.4 mmol) in tetrahydrofuran (one mL) was added to a stirred suspension of sodium hydride (167 mg, 6.95 mmol) in tetrahydrofuran (4 mL). The mixture was heated at 35-40° C. until H2 evolution began. The remaining mixture was added dropwise over about ten minutes. After H2 evolution ceased, part of the solvent was removed under reduced pressure. The residue was diluted with 10 mL of water, neutralized with dilute sulfuric acid and extracted twice with ethyl acetate. The extract was water washed, dried (MgSO4) and stripped to a light brown solid. This was triturated with hexane, filtered and dried to give 1.17 g, (94% yield) of ethyl 3-(4-chlorophenyl)-3-cyano-2-oxopropanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622504B2
Source datasetuspto-grants-2009_11
ORD IDord-a98fdb6960f641cf8096df4b66978b1f
Source noteuspto-grants-2009_11