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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747431Generated: October 31, 2026

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

https://huagongshe.com/reaction/747431

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 numberUS07396848B1
Source datasetuspto-grants-2008_07
ORD IDord-57df518800d84832953d7a2d04975c02
Source noteuspto-grants-2008_07