Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929806Generated: November 1, 2026

2-Fluorophenol → HCID 76281592, compound

https://huagongshe.com/reaction/929806

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluorophenolHCID 9707—
ReactantPotassium CarbonateHCID 11430—
Reactant1613166-38-3HCID 90202460—
SolventAcetonitrileHCID 6342—
ProductHCID 76281592HCID 7628159284%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a mixture of 3-(4-bromomethyl-phenyl)-isoxazole-5-carboxylic acid amide (which may be prepared as described in Preparation of Intermediate 14; 30 mg, 0.107 mmol) in CH3CN (2 mL) were added 2-fluorophenol (16 μL, 0.18 mmol) and K2CO3 (30 mg, 0.22 mmol). The mixture was heated at 90° C. for 16 h and then evaporated to dryness. The residue was purified by chromatography (66-75% EtOAc/hexanes) to give 3-[4-(2-fluoro-phenoxymethyl)-phenyl]-isoxazole-5-carboxylic acid amide (28 mg, 84%) as a white powder. 1H NMR (300 MHz, DMSO-d6) δ ppm 8.38 (br. s., 1H), 8.00 (br. s., 1H), 7.93 (d, J=8.2 Hz, 2H), 7.60 (d, J=7.2 Hz, 3H), 7.17-7.29 (m, 2H), 7.11 (t, J=7.7 Hz, 1H), 6.87-7.01 (m, 1H), 5.25 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296711B2
Source datasetuspto-grants-2016_03
ORD IDord-81797eb1329740eca3533ec49b23e9d0
Source noteuspto-grants-2016_03