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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508159Generated: October 29, 2026

Thionyl Chloride → 4-(Chloromethyl)-2-(4-chloro-3-methylphenyl)-1,3-oxazole

https://huagongshe.com/reaction/508159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant[2-(4-Chloro-3-methylphenyl)-1,3-oxazol-4-yl]methanolHCID 58284347—
SolventDichloromethaneHCID 6344—
Product4-(Chloromethyl)-2-(4-chloro-3-methylphenyl)-1,3-oxazoleHCID 44541971—

Reaction Conditions

Temperature0 °C

Reaction Steps

136 mg (0.61 mmol) of the compound from Example 27A are suspended in 2 ml of dichloromethane. The suspension is cooled to 0° C., and 49 μl (0.67 mmol) of thionyl chloride are added slowly. The reaction solution is stirred at RT overnight. The solvent is then removed on a rotary evaporator. The residue is used without further purification in the subsequent reactions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09095582B2
Source datasetuspto-grants-2015_08
ORD IDord-11fa7d888c304aceb6bce33ccfc5a02c
Source noteuspto-grants-2015_08