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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631570Generated: October 30, 2026

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

https://huagongshe.com/reaction/631570

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 numberUS09320739B2
Source datasetuspto-grants-2016_04
ORD IDord-2303ea23b39047ebb15dc88b77d96f1b
Source noteuspto-grants-2016_04