Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092245Generated: November 1, 2026

Thionyl Chloride → 4-(Chloromethyl)-5-(4-chlorophenyl)-1,3-oxazole

https://huagongshe.com/reaction/2092245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant[5-(4-Chlorophenyl)-1,3-oxazol-4-yl]methanolHCID 58284362—
Product4-(Chloromethyl)-5-(4-chlorophenyl)-1,3-oxazoleHCID 58284264—

Reaction Steps

269 mg (0.77 mmol) of the compound from Example 38A are initially charged in 0.43 ml (5.85 mmol) of thionyl chloride. The reaction mixture is stirred at RT for 12 h, and excess thionyl chloride is then removed under reduced pressure. The residue is taken up in 5 ml of ethyl acetate and washed once with 2 ml of sat. aqueous sodium bicarbonate solution. The organic phase is dried over magnesium sulfate and the solvent is removed on a rotary evaporator. The product obtained is used without further purification in the subsequent reactions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440700B2
Source datasetuspto-grants-2013_05
ORD IDord-1118f9f9eebb4f0eb461148855cad561
Source noteuspto-grants-2013_05