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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395636Generated: October 29, 2026

Phosphorus oxychloride → Ethyl 2-chloro-4-(4-fluorophenyl)-5-oxazolebutanoate

https://huagongshe.com/reaction/395636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantEthyl 4-[4-(4-fluorophenyl)-2-oxo-4-oxazolin-5-yl]butanoateHCID 18174763—
SolventPyridineHCID 1049—
ProductEthyl 2-chloro-4-(4-fluorophenyl)-5-oxazolebutanoateHCID 18174687—

Reaction Conditions

Temperature125 °C

Reaction Steps

A mixture of ethyl 4-[4-(4-fluorophenyl)-2-oxo-4-oxazolin-5-yl]butanoate (7.00 g), phosphorus oxychloride (14.7 g) and pyridine (1.89 g) was heated to 120-130° C. and stirred for 45 minutes. The reaction mixture was poured into ice water (200 ml) and extracted with ethyl acetate (150 ml×2). The organic layer was washed in sequence with a 10% aqueous solution of sodium hydrogen carbonate (100 ml) and a saturated aqueous solution of sodium chloride (100 ml), and then dried over anhydrous magnesium sulfate. The organic layer was concentrated, the residue was subjected to silica gel column chromatography, and ethyl 2-chloro-4-(4-fluorophenyl)-5-oxazolebutanoate was obtained as a yellow oil (4.23 g, 57%) from an ethyl acetate-hexane (1:4, v/v)-eluted fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605629B1
Source datasetuspto-grants-2003_08
ORD IDord-14f57682ce434a61be0b0fc625a3ced5
Source noteuspto-grants-2003_08