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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295216Generated: November 1, 2026

Ethyl Acetate → 4-(3-Chloromethyl-5-ethoxyphenoxymethyl)-5-methyl-2-phenyloxazole

https://huagongshe.com/reaction/1295216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantThionyl ChlorideHCID 24386—
Reactant3-Ethoxy-5-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyl alcoholHCID 69427333—
SolventTolueneHCID 1140—
Product4-(3-Chloromethyl-5-ethoxyphenoxymethyl)-5-methyl-2-phenyloxazoleHCID 2293067992%

Reaction Steps

To a solution of 3-ethoxy-5-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyl alcohol (4.38 g) in toluene (80 ml) was added dropwise thionyl chloride (1.69 g) at room temperature. After stirring for 90 min, ethyl acetate (100 ml) was added to the reaction mixture and the mixture was washed with aqueous sodium bicarbonate and then with water. The organic layer was dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography, and the crystals obtained from the fraction eluted with ethyl acetate-hexane (1:4, volume ratio) were recrystallized from ethyl acetate-hexane to give 4-(3-chloromethyl-5-ethoxyphenoxymethyl)-5-methyl-2-phenyloxazole (4.25 g, 92%) as colorless prism crystals. melting point: 86–87° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241785B2
Source datasetuspto-grants-2007_07
ORD IDord-24e6ff999b2f448fa86a8917b7447581
Source noteuspto-grants-2007_07