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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 233078Erstellt: 25. Oktober 2026

Benzyl Alcohol → 2-Furancarboxylic acid, tetrahydro-, phenylmethyl ester

https://huagongshe.com/reaction/233078

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl AlcoholHCID 244—
EduktPyridineHCID 1049—
EduktTetrahydro-2-furancarbonyl chlorideHCID 551254—
LösungsmittelDiethyl EtherHCID 3283—
Produkt2-Furancarboxylic acid, tetrahydro-, phenylmethyl esterHCID 11287208—

Reaktionsschritte

Tetrahydrofuroyl chloride (15.0 g, 112 mmol) was added dropwise to a cold solution of benzyl alcohol (10.9 g, 101 mmol) and pyridine (20.0 g, 253 mmol) in Et2O (200 mL). The solution was stirred at 0° for 40 minutes, then filtered to remove the side product pyridine hydrochloride. The filtrate was washed with 0.1M HCl (50 mL), saturated aqueous NaHCO3 (50 mL), and brine (50 mL), and then dried over MgSO4. Filtration and evaporation of the solvent gave a yellow oil, which was distilled. Benzyl tetrahydrofuroate was obtained as a colorless oil (21.1 g), b.p. 118° to 120° at 0.5 mm Hg.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05591846
Quelldatensatzuspto-grants-1997_01
ORD IDord-4d9fe164f77e42d2b03cb5c0f4ea08e2
Quellennotizuspto-grants-1997_01