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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8200Generated: October 25, 2026

Boron trifluoride etherate → 4-(5-Oxo-tetrahydro-furan-3-yl)-benzoic Acid Ethyl Ester

https://huagongshe.com/reaction/8200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant4-(5-Methoxy-tetrahydro-furan-3-yl)-benzoic Acid Ethyl EsterHCID 69365300—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product4-(5-Oxo-tetrahydro-furan-3-yl)-benzoic Acid Ethyl EsterHCID 69363763—

Reaction Steps

To a solution of 75% 3-chloroperbenzoic acid (2.7 g, 11.76 mmol) in dichloromethane (35 mL) is added magnesium sulfate (2.0 g, 16.6 mmol) and the mixture stirred for 30 min. Solids are removed by filtration and the filtrate treated with borontrifluoride etherate (0.5 mL, 3.92 mmol) and 4-(5-methoxy-tetrahydro-furan-3-yl)-benzoic acid ethyl ester (2.45 g, 9.8 mmol) in dichloromethane (5 mL). The mixture is stirred at room temperature 18 h, diluted with ether (200 mL) and washed with a 10% solution of sodium thiosulfite (150 mL), a saturated solution of sodium bicarbonate (150 mL) and brine. The mixture is dried over magnesium sulfate, filtered and concentrated in vacuo. The residue is chromatographed on SiO2 (elute with 20% ethyl acetate/hexanes) to yield the title compound, 2.2 g (96%), as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087626B2
Source datasetuspto-grants-2006_08
ORD IDord-533050e5611d4df3b3683b95512ad06a
Source noteuspto-grants-2006_08