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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279446Generated: October 30, 2026

Sulfuric Acid → 2-(2,5-Dimethylphenoxymethyl)phenyl isoxazol-3-yl ketone

https://huagongshe.com/reaction/279446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantEthyl BromideHCID 6332—
ReactantMagnesiumHCID 5462224—
Reactant2-Bromobenzyl-(2,5-dimethylphenyl)etherHCID 10946216—
Reactant1,2-Oxazole-3-carbonitrileHCID 22624610—
SolventTetrahydrofuranHCID 8028—
Product2-(2,5-Dimethylphenoxymethyl)phenyl isoxazol-3-yl ketoneHCID 109028756.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

THF (2 ml) and bromoethane (0.1 ml) were added to magnesium (0.49 g, 0.02 mol) in a stream of nitrogen, and the mixture was stirred at 50° C. for 10 minutes. Then, a mixture of 1-bromo-2-(2,5-dimethylphenoxymethyl)benzene (2.91 g, 0.01 mol) and THF (8 ml) was added at 50 to 60° C. over 30 minutes, and the mixture was stirred at 50 to 60° C. for 1 hour. After completion of the reaction, the reaction mixture was added to a mixture of 3-cyanoisoxazole (1.45 g, 0.015 mol) and THF (15 ml) at 20° C. or lower over 15 minutes, and then the mixture was stirred at room temperature for 2 hours. After completion of the reaction, 2N sulfuric acid (200 ml) was added, and the mixture was extracted with ether. The ether layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure, and the residue was purified by silica gel chromatography (ethyl acetate/n-hexane) and recrystallized from n-hexane to give 2-(2,5-dimethylphenoxymethyl)phenyl isoxazol-3-yl ketone (0.20 g, 6.3%) as colorless crystals. mp. 90.5-92° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362212B1
Source datasetuspto-grants-2002_03
ORD IDord-4aeffda511844029a092d2c64a9a3057
Source noteuspto-grants-2002_03