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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918558Generated: October 31, 2026

1,2-Dimethoxyethane → Ethyl 5-(2,5-difluorobenzyl)isoxazole-3-carboxylate

https://huagongshe.com/reaction/1918558

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium CarbonateHCID 10340—
Reactant(2,5-Difluorophenyl)boronic acidHCID 2734335—
ReactantEthyl 5-(bromomethyl)-1,2-oxazole-3-carboxylateHCID 13124955—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
ProductEthyl 5-(2,5-difluorobenzyl)isoxazole-3-carboxylateHCID 6683191559%

Reaction Steps

1,2-Dimethoxyethane (8 mL) and water (2 mL) were added to the mixture of ethyl 5-(bromomethyl)isoxazole-3-carboxylate (1.00 g; 4.27 mmol), 2,5-difluorophenylboronic acid (0.773 g; 4.70 mmol), tetrakis(triphenylphosphine)palladium(0) (0.248 g; 0.640 mmol) and sodium carbonate (0.911 g; 8.55 mmol). The mixture was irradiated in a microwave oven at 130° C. for 20 minutes. After cooling, the reaction mixture was extracted with ethyl acetate and water. The organic layer was concentrated under reduced pressure and the residue was purified by flash chromatography on silica gel (eluent: 5 to 40% of ethyl acetate in heptane) to give 0.67 g (59%) of ethyl 5-(2,5-difluorobenzyl)isoxazole-3-carboxylate as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618138B2
Source datasetuspto-grants-2013_12
ORD IDord-9801bf5490884015ae1f168f8ad3998b
Source noteuspto-grants-2013_12