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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 8200Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/8200

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBoron trifluoride etherateHCID 8000—
EduktSulfuric acid magnesium salt (1:1)HCID 24083—
Eduktm-Chloroperbenzoic acidHCID 70297—
Edukt4-(5-Methoxy-tetrahydro-furan-3-yl)-benzoic Acid Ethyl EsterHCID 69365300—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-(5-Oxo-tetrahydro-furan-3-yl)-benzoic Acid Ethyl EsterHCID 69363763—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087626B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-533050e5611d4df3b3683b95512ad06a
Quellennotizuspto-grants-2006_08