Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871621Generated: October 31, 2026

Potassium Carbonate → 4-Chlorophenyl 3-(2-fluoropropan-2-yl)isoxazol-5-ylcarbamate

https://huagongshe.com/reaction/871621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chlorophenyl chloroformateHCID 139059—
Reactant3-(2-Fluoropropan-2-yl)-1,2-oxazol-5-amineHCID 53402070—
SolventTetrahydrofuranHCID 8028—
Product4-Chlorophenyl 3-(2-fluoropropan-2-yl)isoxazol-5-ylcarbamateHCID 6687752171%

Reaction Steps

3-(2-fluoropropan-2-yl)isoxazol-5-amine (11.26 g, 78.19 mmol) described in Example 42A in THF (300 mL) was treated with potassium carbonate (21.58 g, 156 mmol) and p-chlorophenyl chloroformate (14.94 g, 78.19 mmol). After stirring at rt for 1 h, additional p-chlorophenyl chloroformate (7.5 g, 39.26 mmol) was introduced, and the reaction mixture was stirred at rt overnight. The mixture was filtered through a celite pad, washed with ethyl acetate and concentrated to dryness. The residue was taken into ethyl acetate, washed with brine, and the organics dried (MgSO4) and concentrated. The residue was purified by silica gel chromatography (eluting with 10 to 50% ethyl acetate in hexanes) to give 4-chlorophenyl 3-(2-fluoropropan-2-yl)isoxazol-5-ylcarbamate (16.51 g, 71%) as a cream solid. 1H NMR (300 MHz, CDCl3) δ 7.87 (brs, 1H), 7.36-7.41 (m, 2H), 7.13-7.17 (m, 2H), 6.27 (s, 1H), 1.74 (d, J=21 Hz, 6H); LC-MS (ESI) m/z 299 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969587B2
Source datasetuspto-grants-2015_03
ORD IDord-a05aafda311e477eacc3099dc690aa5c
Source noteuspto-grants-2015_03