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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477581Generated: October 30, 2026

Ethyl Acetate → HCID 15080947, compound

https://huagongshe.com/reaction/477581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantST50306943HCID 2725017—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
ProductHCID 15080947HCID 15080947—

Reaction Steps

In 20 ml of ethyl acetate was dissolved 0.73 g of 2,3,4-tri-O-acetyl-1-azido-1-deoxy-β-D-xylopyranose, and 65 mg of 10% Pd/C was added to the solution. Then the solution was stirred in a hydrogen atmosphere for 2 hours. The Pd/C was removed by filtration, and the filtrate was concentrated. To the concentrate was added 20 ml of pyridine, 3 ml of acetic anhydride and then 10 mg of 4-dimethylaminopyridine, and the mixture was stirred for 16 hours. Water was added to the reaction, and the mixture was extracted with chloroform. The chloroform layer was washed with 0.1 N HCl solution, 1% sodium bicarbonate solution and finally with water, dehydrated and concentrated. The residue was subjected to silica gel column chromatography with a system of chloroform-acetone (100:1) to obtain 0.4 mg of 1-acetamido-2,3,4-tri-O-acetyl-1-deoxy-β-D-xylopyranose.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04888418
Source datasetuspto-grants-1989_12
ORD IDord-abf8a18776d74fac8ee5c29c0bdd667e
Source noteuspto-grants-1989_12