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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716857Generated: November 2, 2026

Thionyl Chloride → Ethyl 2-[4-(chloromethyl)phenyl]-1,3-oxazole-4-carboxylate

https://huagongshe.com/reaction/1716857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantEthyl 2-[4-(hydroxymethyl)phenyl]-1,3-oxazole-4-carboxylateHCID 46834789—
ReactantHCID 178418385HCID 178418385—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-[4-(chloromethyl)phenyl]-1,3-oxazole-4-carboxylateHCID 4683479082%

Reaction Steps

A solution of ethyl 2-[4-(hydroxymethyl)phenyl]-1,3-oxazole-4-carboxylate (0.467 g, 1.89 mmol) in CH2Cl2 was treated with a solution of thionyl chloride (0.281 g, 2.36 mmol) and benzotriazole (0.281 g, 2.36 mmol) in CH2Cl2, and stirred 6 hours at room temperature. The reaction was diluted with CHCl3, filtered over Celite and concentrated under vacuum. The resultant residue was purified by flash chromatography (silica, MeOH:CH2Cl2 5%) to give the title product in 82% yield, identified by NMR and mass spectral analyses. LCMS (ESI+) 266 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803825B2
Source datasetuspto-grants-2010_09
ORD IDord-f149aedecfa84eb0a80e0ed0eacee0a5
Source noteuspto-grants-2010_09