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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857322Generated: October 25, 2026

Phenacyl bromide → 4-[3-(4,5-Dihydroisoxazol-3-yl)-4-methylsulfonyl-2-methylbenzoyl]-1-ethyl-5-phenacyloxypyrazole

https://huagongshe.com/reaction/1857322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178463114HCID 178463114—
SolventDimethylformamideHCID 6228—
Product4-[3-(4,5-Dihydroisoxazol-3-yl)-4-methylsulfonyl-2-methylbenzoyl]-1-ethyl-5-phenacyloxypyrazoleHCID 1547745764.7%

Reaction Steps

0.20 g of 4-[3-(4,5-dihydroisoxazol-3-yl)-4-methylsulfonyl-2-methylbenzoyl]-1-ethyl-5-hydroxypyrazole was dissolved in 10 ml of DMF, and 0.11 g of potassium carbonate, then 0.13 g of phenacyl bromide were added. The resulting solution was stirred at room temperature overnight. The reaction solution was poured into ice water, and extracted with ethyl acetate. The organic layer was washed with water, then with a saturated sodium chloride solution, and dried over anhydrous magnesium sulfate. The solvent was distilled out under reduced pressure. Methanol was added to the residue. The obtained crystals were separated by filtration to give 0.17 g of the title compound as white crystals. m.p. 177~179° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06147031
Source datasetuspto-grants-2000_11
ORD IDord-abb9c3034bb7408e91264ea05b3bd8b6
Source noteuspto-grants-2000_11