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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413044Generated: November 1, 2026

Benzene → 1-propenyl 3-O-benzyl-2-deoxy-2-palmitamido-6-O-palmitoyl-beta-D-glucopyranoside

https://huagongshe.com/reaction/2413044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantEthanolHCID 702—
ReactantDabcoHCID 9237—
ReactantAllyl 3-O-benzyl-2-deoxy-2-palmitamido-6-O-palmitoyl-beta-D-glucopyranosideHCID 18595872—
CatalystChlorotris(triphenylphosphine)rhodium(I)HCID 84599—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product1-propenyl 3-O-benzyl-2-deoxy-2-palmitamido-6-O-palmitoyl-beta-D-glucopyranosideHCID 54429339—

Reaction Steps

To 500 mg. of Compound 6 in a mixture of 2.0 ml. of ethanol, benzene and water (7:3:1) 40 mg. of tris(triphenylphosphine)rhodium(I) chloride and 15 mg. of 1,4-diazabicyclo-[2.2.2]octane were added. The reaction mixture was heated under reflux overnight. Thin layer chromatography (5% acetone in CHCl3) showed the reaction to be complete. The reaction was conducted in the general manner described by Corey et al, in J. Org. Chem., 38 (1973) 3224 and P. A. Gent et al, J. Chem. Soc., Chem. Commun., (1974) 277-278. A high yield of Compound 7 was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04495346
Source datasetuspto-grants-1985_01
ORD IDord-9f71ab1a46774860b95d66d044bec2b9
Source noteuspto-grants-1985_01