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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1786641Erstellt: 24. Oktober 2026

Triethylamine → n-Galactosylgeranamide

https://huagongshe.com/de/reaction/1786641

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktIsobutyl chloroformateHCID 62365—
EduktD-(+)-Galactosamine hydrochlorideHCID 2723866—
EduktGeranic acidHCID 5275520—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelSodium HydroxideHCID 14798—
Produktn-GalactosylgeranamideHCID 6713392946%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a THF (20 ml) solution containing geranic acid (0.84 g, 5 mmols), triethylamine (0.51 g, 5 mmols) was added and cooled to 0° C., into which a THF (5 ml) solution containing isobutyl chloroformate (0.68 g, 5 mmols) was added dropwise, followed by 30 minutes' stirring at 0° C. Then galactosamine hydrochloride (1.08 g, 5 mmols) was dissolved in 10 ml of water, to which 5 ml of 1N sodium hydroxide was further added, and the solution was added to the reaction mixture all at a time. After the following stirring for an hour at 0° C. and for further 4 hours at room temperature, the reaction mixture was condensed under reduced pressure. To the residue 150 ml of acetone was added and precipitated sodium chloride was filtered off. The filtrate was condensed once again and the residue was separated on silica gel column chromatography. Consequently the product was obtained from the hexane-ethanol (2:1) distillate as a viscous oily substance, to which a minor amount of ether was added to crystallize the product. Through subsequent suction filtration, 0.754 g of the title compound was obtained. The yield was 46%, and the melting point was 85-87° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07507765B2
Quelldatensatzuspto-grants-2009_03
ORD IDord-281f019ab44e493bac9d647da6402ad8
Quellennotizuspto-grants-2009_03