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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929978Generated: October 30, 2026

Water → Phenyl 3-(2-fluoropropan-2-yl)isoxazol-5-ylcarbamate

https://huagongshe.com/reaction/929978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantPhenyl chloroformateHCID 15891—
Reactant3-(2-Fluoropropan-2-yl)-1,2-oxazol-5-amineHCID 53402070—
SolventTetrahydrofuranHCID 8028—
ProductPhenyl 3-(2-fluoropropan-2-yl)isoxazol-5-ylcarbamateHCID 6687662676%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 3-(2-fluoropropan-2-yl)isoxazol-5-amine (4.32 g, 0.03 mol) and K2CO3 (8.28 g, 0.06 mol) in THF (100 mL) at 0° C. was added dropwise a solution of phenyl carbonochloridate (6 mL, 0.045 mol) in THF (50 mL). The mixture was stirred at 0° C. for 1 h, then at 40° C. for 20 h. Analysis by LC-MS and TLC indicated that the starting material was almost completely consumed and a new product had formed. The mixture was poured into water (150 mL) and the resulting mixture was extracted with EtOAc (100 mL). The organic layer was dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by silica gel chromatography eluting with 0-4% EtOAc in petroleum ether to afford phenyl 3-(2-fluoropropan-2-yl)isoxazol-5-ylcarbamate as a white solid (6 g, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296722B2
Source datasetuspto-grants-2016_03
ORD IDord-d63e6e52879e4b06bb21a551689e6869
Source noteuspto-grants-2016_03