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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424534Generated: October 25, 2026

Sodium Carbonate → 5-(4-Cyano-2-fluoro-phenyl)-isoxazole-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1424534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Cyano-2-Fluorophenylboronic AcidHCID 44755209—
ReactantEthyl 5-chloro-1,2-oxazole-3-carboxylateHCID 66831968—
Solvent1,4-DioxaneHCID 31275—
Product5-(4-Cyano-2-fluoro-phenyl)-isoxazole-3-carboxylic acid ethyl esterHCID 71093733—

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 5-chloro-isoxazole-3-carboxylic acid ethyl ester (600 mg), 4-cyano-2-fluorophenylboronic acid (665 mg), and aqueous Na2CO3 solution (2 M; 4.41 mL) in 1,4-dioxane (15 mL) is purged with argon for 15 min prior to the addition of Pd(PPh3)4 (276 mg). The reaction mixture is heated under an argon atmosphere to 140° C. for 20 min in a microwave oven. The solvent is evaporated in vacuo and the residue is mixed with water and ethyl acetate. The aqueous phase is extracted with ethyl acetate and the combined extracts are washed with brine, dried over MgSO4 and concentrated in vacuo. The crude product is purified by silica gel chromatography (cyclohexane/ethyl acetate 80:20→50:50). LC (method 3): tR=1.50 min; Mass spectrum (ESI+): m/z=261 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927726B2
Source datasetuspto-grants-2015_01
ORD IDord-ebda754e58264352ba8eb380841b441d
Source noteuspto-grants-2015_01