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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612931Generated: October 30, 2026

Acetyl chloride → 3-(2-Acetylaminoethoxy)-5-phenylisoxazole

https://huagongshe.com/reaction/612931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant3-(2-Aminoethoxy)-5-phenylisoxazole hydrochlorideHCID 9859596—
SolventTetrahydrofuranHCID 8028—
Product3-(2-Acetylaminoethoxy)-5-phenylisoxazoleHCID 1959664491.6%

Reaction Conditions

Temperature5 °C

Reaction Steps

3-(2-Aminoethoxy)-5-phenylisoxazole hydrochloride (240 mg) was suspended in anhydrous tetrahydrofuran (5 ml), and the suspension was cooled to 5° C. Acetyl chloride (94 mg) and triethylamine (243 mg) were added thereto, and the resulting mixture was stirred at the same temperature for 30 minutes. At the end of this time, the reaction mixture was added to ice-cold water (40 ml) and extracted with ethyl acetate (40 ml×2). Then, the organic layer was dried over anhydrous magnesium sulfate. After filtration, the solvent was evaporated under reduced pressure. The crystals thus obtained were recrystallized from ethyl acetate to obtain the title compound (225 mg, 91%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06005116
Source datasetuspto-grants-1999_12
ORD IDord-84ef6243f83242e7bb262a067f2fb6ff
Source noteuspto-grants-1999_12