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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553684Generated: October 31, 2026

Triethylamine → [5-(4-Bromo-phenyl)-3-methyl-isoxazol-4-yl]-carbamic acid 1-(2-fluoro-phenyl)-ethyl ester

https://huagongshe.com/reaction/553684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Fluoro-alpha-methylbenzenemethanolHCID 123066—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant5-(4-Bromophenyl)-3-methyl-1,2-oxazole-4-carboxylic acidHCID 56604559—
SolventTolueneHCID 1140—
Product[5-(4-Bromo-phenyl)-3-methyl-isoxazol-4-yl]-carbamic acid 1-(2-fluoro-phenyl)-ethyl esterHCID 67352942—

Reaction Steps

5-(4-Bromo-phenyl)-3-methyl-isoxazole-4-carboxylic acid (4 g, 14.2 mmol) was dissolved in toluene (150 mL). Triethylamine (2.187 mL, 15.6 mmol) was added, followed by diphenylphosphoryl azide (3.372 mL, 15.6 mmol), and the mixture was stirred for 10 minutes. 2-Fluoro-alpha-methylbenzyl alcohol (2 g, 15.6 mmol) was added, and the reaction was stirred at 80° C. overnight. The mixture was cooled to room temperature and concentrated, and the residue was partitioned between with EtOAc and water. The organic layer was washed 4 times with water and once with brine, and then dried, filtered, and concentrated, and the residue was purified by silica gel chromatography (dry load; 0-100% EtOAc in hexanes) to give [5-(4-bromo-phenyl)-3-methyl-isoxazol-4-yl]-carbamic acid 1-(2-fluoro-phenyl)-ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048902B2
Source datasetuspto-grants-2011_11
ORD IDord-dfb13a6b993e49309c164033a2866377
Source noteuspto-grants-2011_11