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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | 3-(2-Fluoropropan-2-yl)-1,2-oxazol-5-amine | HCID 53402070 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Phenyl 3-(2-fluoropropan-2-yl)isoxazol-5-ylcarbamate | HCID 66876626 | 76% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09296722B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-d63e6e52879e4b06bb21a551689e6869 |
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| Source note | uspto-grants-2016_03 |
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