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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747438Generated: October 27, 2026

Pyridine → Methyl 2-chloro-4-(4-trifluoromethylphenyl)-5-oxazolepropionate

https://huagongshe.com/reaction/747438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantMethyl 3-[2-oxo-4-(4-trifluoromethylphenyl)-4-oxazolin-5-yl]propionateHCID 23431800—
SolventWaterHCID 962—
ProductMethyl 2-chloro-4-(4-trifluoromethylphenyl)-5-oxazolepropionateHCID 23431805—

Reaction Conditions

Temperature102.5 °C

Reaction Steps

A mixture of methyl 3-[2-oxo-4-(4-trifluoromethylphenyl)-4-oxazolin-5-yl]propionate (3.90 g), phosphorus oxychloride (11.5 g) and pyridine (0.98 g) was heated to 100-105° C. and stirred for 1 hour. The reaction mixture was added dropwise to heated water (100 ml) of 30° C. and extracted with ethyl acetate (150 ml×2). The organic layer was washed with a saturated aqueous solution of sodium chloride (100 ml), and dried over anhydrous magnesium sulfate. The organic layer was concentrated, the residue was subjected to silica gel column chromatography, and methyl 2-chloro-4-(4-trifluoromethylphenyl)-5-oxazolepropionate was obtained as a yellow oil (2.66 g, 64%) 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-3c53901a7dbe4b28bd36fb97ec690dfa
Source noteuspto-grants-2008_07