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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1612997Erstellt: 26. Oktober 2026

Furan → 1-Oxo-1-furyl-7-methoxycarbonyl-4-heptyne

https://huagongshe.com/reaction/1612997

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFuranHCID 8029—
EduktAcetic acid, 2,2-dichloro-, 1,1'-anhydrideHCID 77772—
Edukt6-Methoxycarbonyl-1-carboxy-3-hexyneHCID 10976151—
LösungsmittelTolueneHCID 1140—
Produkt1-Oxo-1-furyl-7-methoxycarbonyl-4-heptyneHCID 1102081265%

Reaktionsschritte

A mixture of 6-methoxycarbonyl-1-carboxy-3-hexyne [VI-1] (18.4 g, 0.1 mole), furan (13.6 g, 0.2 mole), dichloroacetic anhydride (28.8 g, 0.12 mole), boron trifluoride ether complex (3.2 g) and toluene (100 ml) is reacted at 20°-30° C. for 10 hours. After completion of the reaction, the reaction mixture is cooled, washed successively with water, 5% aqueous sodium carbonate solution and water, and the organic layer is dried over anhydrous magnesium sulfate. The dried organic layer is concentrated under reduced pressure, and the resulting residue is purified by silica gel column chromatography to give 1-oxo-1-furyl-7-methoxycarbonyl-4-heptyne [VII-1] (15.2 g, yield; 65%), b.p. 120°-125° C./0.8 mmHg.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05191109
Quelldatensatzuspto-grants-1993_03
ORD IDord-fec77589ac0e4266aa815806a342106b
Quellennotizuspto-grants-1993_03