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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105703Generated: October 26, 2026

Triethylamine → n-Galactosylgeranamide

https://huagongshe.com/reaction/2105703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
ReactantD-(+)-Galactosamine hydrochlorideHCID 2723866—
ReactantGeranic acidHCID 5275520—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
Productn-GalactosylgeranamideHCID 6713392946%

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579376B2
Source datasetuspto-grants-2009_08
ORD IDord-fd5ade65301143d6b674f270b93b28f7
Source noteuspto-grants-2009_08