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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295232Generated: October 31, 2026

Thionyl Chloride → 5-Chloromethyl-3-(5-methyl-2-phenyl-4-oxazolylmethoxy)isoxazole

https://huagongshe.com/reaction/1295232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(5-Methyl-2-phenyl-4-oxazolylmethoxy)-5-isoxazolylmethanolHCID 17861205—
SolventTolueneHCID 1140—
Product5-Chloromethyl-3-(5-methyl-2-phenyl-4-oxazolylmethoxy)isoxazoleHCID 1786128589%

Reaction Steps

To a solution of 3-(5-methyl-2-phenyl-4-oxazolylmethoxy)-5-isoxazolylmethanol (2.86 g) in toluene (50 ml) was slowly added thionyl chloride (0.80 ml) at room temperature and the mixture was stirred under reflux for 30 min. After cooling, the reaction mixture was poured into saturated aqueous sodium hydrogen carbonate and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated to give 5-chloromethyl-3-(5-methyl-2-phenyl-4-oxazolylmethoxy)isoxazole (2.70 g, yield 89%) as colorless crystals. The crystals were recrystallized from ethyl acetate-hexane. melting point: 105–106° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241785B2
Source datasetuspto-grants-2007_07
ORD IDord-b8a3e1ca133f4a22b6a6f97fc1a9292c
Source noteuspto-grants-2007_07