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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182822Generated: November 1, 2026

Dichloromethane → 4-(Chloromethyl)-2-(furan-2-yl)-5-methyl-1,3-oxazole

https://huagongshe.com/reaction/1182822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant2-(2-Furyl)-5-methyl-4-oxazolylmethanolHCID 17861204—
SolventWaterHCID 962—
Product4-(Chloromethyl)-2-(furan-2-yl)-5-methyl-1,3-oxazoleHCID 2234458231%

Reaction Steps

The dichloromethane (1 mL) solution of {2-(furan-2-yl)-5-methyloxazol-4-yl}methanol (36 mg, 0.2 mmol), N,N-dimethylaminopyridine (37 mg, 0.3 mmol) and p-toluene sulfonyl chloride (57 mg, 0.3 mmol) was stirred at 60° C. for 2 hrs. The reaction mixture was added water and extracted with ethyl acetate. The organic layer was combined, washed with water and brine, dried over anhydrous sodium sulfate, and concentrated in vacuo. The resulting residues were subjected to silica gel column chromatography (hexane/ethyl acetate) to obtain 4-(chloromethyl)-2-(furan-2-yl)-5-methyloxazole (13 mg, 31%) as a transparent oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664226B2
Source datasetuspto-grants-2014_03
ORD IDord-7fba429e75f04240aadfd731009a9fdb
Source noteuspto-grants-2014_03