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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918514Generated: October 26, 2026

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

https://huagongshe.com/reaction/1918514

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium CarbonateHCID 10340—
Reactant3-Fluorophenylboronic acidHCID 2733986—
ReactantEthyl 5-(bromomethyl)-1,2-oxazole-3-carboxylateHCID 13124955—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
ProductEthyl 5-(3-fluorobenzyl)isoxazole-3-carboxylateHCID 6683176861%

Reaction Steps

1,2-Dimethoxyethane (8 mL) and water (2 mL) were added to the mixture of ethyl 5-(bromomethyl)isoxazole-3-carboxylate (0.710 g; 3.03 mmol), 3-fluorophenylboronic acid (0.481 g; 3.34 mmol), tetrakis(triphenylphosphine)palladium(0) (0.176 g; 0.151 mmol) and sodium carbonate (0.646 g, 6.07 mmol). The mixture was irradiated in a microwave oven at 130° C. for 15 min and was evaporated. The residue was partitioned between dichloromethane (30 mL) and brine (20 mL). The organic layer was separated and concentrated. The residue was purified by flash chromatography on silica gel (eluent: 15 to 100% of dichloromethane in heptane) to afford 0.460 g (61%) of ethyl 5-(3-fluorobenzyl)isoxazole-3-carboxylate as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618138B2
Source datasetuspto-grants-2013_12
ORD IDord-0b0fec1202ba40ad995b2898679172c5
Source noteuspto-grants-2013_12