Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929790Generated: October 31, 2026

2-Chlorophenol → 3-[4-(2-Chloro-phenoxymethyl)-phenyl]-isoxazole-5-carboxylic acid amide

https://huagongshe.com/reaction/929790

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorophenolHCID 7245—
ReactantPotassium CarbonateHCID 11430—
Reactant1613166-38-3HCID 90202460—
SolventAcetonitrileHCID 6342—
Product3-[4-(2-Chloro-phenoxymethyl)-phenyl]-isoxazole-5-carboxylic acid amideHCID 7628079979.3%

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; 40 mg, 0.142 mmol) in CH3CN (2 mL) were added 2-chlorophenol (22 μL, 0.22 mmol) and K2CO3 (40 mg, 0.29 mmol). The mixture was heated at 90° C. for 4 h and then evaporated to dryness. The residue was purified by chromatography (66-75% EtOAc/hexanes) to give 3-[4-(2-chloro-phenoxymethyl)-phenyl]-isoxazole-5-carboxylic acid amide (37 mg, 79%) as a white solid. 1H NMR (300 MHz, DMSO-d6) δ ppm 8.39 (br. s., 1H), 8.01 (br. s., 1H), 7.94 (d, J=8.1 Hz, 2H), 7.61 (d, J=9.5 Hz, 3H), 7.44 (dd, J=8.1, 1.5 Hz, 1H), 7.19-7.35 (m, 2H), 6.92-7.01 (m, 1H), 5.29 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296711B2
Source datasetuspto-grants-2016_03
ORD IDord-a75722f35d2d408faf17d7148c95615b
Source noteuspto-grants-2016_03