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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441714Generated: October 31, 2026

Thionyl Chloride → Ethyl 2-methyl-5-(2-phenylethyl)-1,3-oxazole-4-carboxylate

https://huagongshe.com/reaction/441714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 21417731HCID 21417731—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-methyl-5-(2-phenylethyl)-1,3-oxazole-4-carboxylateHCID 21417734—

Reaction Steps

To the entire oily residue obtained in Step A is added at 0° C., 60 ml. of thionyl chloride and the resulting mixture refluxed for 40 minutes. The reaction mixture is then cooled and evaporated (under vacuum) to obtain a residue. The residue is dissolved in methylene chloride, and the solution washed with 5% aqueous sodium bicarbonate (100 ml.). The organic layer is then dried over anhydrous sodium sulfate and evaporated (under vacuum) to obtain the title compound as a crude residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04042596
Source datasetuspto-grants-1977_08
ORD IDord-babd5c12c6cb4fdbb5ec5fcfdfdfe03c
Source noteuspto-grants-1977_08