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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 43316Erstellt: 23. Oktober 2026

Potassium Hydroxide → 4-(Tetrahydrofuran-3-yl)-3-buten-2-one

https://huagongshe.com/de/reaction/43316

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
EduktDimethyl (2-oxopropyl)phosphonateHCID 77872—
Edukt3-Furancarboxaldehyde, tetrahydro-HCID 157568—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produkt4-(Tetrahydrofuran-3-yl)-3-buten-2-oneHCID 67177193—

Reaktionsschritte

Dimethyl (2-oxopropyl)phosphonate (32.06 g, 193 mmol) is added to a chilled (ice-bath) solution of potassium hydroxide (10.83 g, 193 mmol) in water (30 ml) and ethanol (170 ml) and the mixture is stirred. Tetrahydrofuran-3-carboxaldehyde (50% wt. % solution in water, 25 ml, 138 mmol) is added dropwise and the reaction mixture is stirred at 5° C. for 10 minutes. The cooling bath is removed and the mixture is stirred at room temperature for 7 hours. Most of the solvent is removed in vacuo, water (100 ml) and diethyl ether (200 ml) are added, the mixture is poured into a separating funnel and the organic phase collected. The aqueous phase is extracted three times with diethyl ether, and the organic extracts are combined, dried over anhydrous magnesium sulphate, filtered and the filtrate is evaporated in vacuo. The residue is further purified by column chromatography on silica gel, eluting with a mixture of ethyl acetate and hexane to give 4-(tetrahydrofuran-3-yl)-3-buten-2-one as a pale yellow liquid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536351B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-cafd4c47a9d24c2c85dda39dc24b23e0
Quellennotizuspto-grants-2013_09