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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817300Generated: October 27, 2026

Chloroform → Ethyl 5-butoxy-1,3-oxazole-2-carboxylate

https://huagongshe.com/reaction/1817300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantEthyl AcetateHCID 8857—
ReactantPhosphorus oxide (P4O10)HCID 14812—
Reactantbutyl N-[ethoxy(oxo)acetyl]glycinateHCID 69643286—
SolventAcetonitrileHCID 6342—
SolventSodium chloride; waterHCID 57417360—
ProductEthyl 5-butoxy-1,3-oxazole-2-carboxylateHCID 66996945—

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of P2O5 (22 g, 155.6 mmol) in CH3CN (50 mL) under nitrogen was warmed to 50° C. and treated with butyl N-[ethoxy(oxo)acetyl]glycinate (6 g, 25.9 mmol) dissolved in 10 mL CH3CN. The mixture was heated to 65° C. for 1.5 hours, then cooled in an ice bath. Ice and brine were added to the reaction mixture, then EtOAc was added and the mixture transferred to a separatory funnel. CHCl3 was added to dissolve solids and the organic layer was isolated. The aqueous layer was washed repeatedly with CHCl3 and EtOAc, the organic layers were combined and dried with Na2SO4, then concentrated. The residue was chromatographed on silica eluting with a gradient of 0-30% EtOAc/Hexanes to give the product as a clear, colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598264B2
Source datasetuspto-grants-2009_10
ORD IDord-f2dc169bf52842899053df8afcd8fa41
Source noteuspto-grants-2009_10