Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858879Generated: October 31, 2026

Pyridine → HCID 131721483, compound

https://huagongshe.com/reaction/1858879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 131721484HCID 131721484—
SolventDichloromethaneHCID 6344—
ProductHCID 131721483HCID 13172148393%

Reaction Steps

Ethyl 2,3-O-dibenzoyl-4-O-benzyl-1-thio-β-D-glucohexopyranoside (200 mg, 0.38 mmol) was dissolved in an ice-cooled mixture of pyridine and acetic anhydride (1:1, 6 Å). The mixture was stirred and attained at room temperature overnight. The mixture was diluted with dichloromethane, washed with satd. aq. sodium hydrogen carbonate and water and dried over sodium sulphate. The solvents were removed under reduced pressure and the residue was subjected to flash chromatography on silica gel (toluene-acetonitrile 6:1) to yield 204 mg, 93% of ethyl 6-O-acetyl-2,3-O-dibenzoyl-4-O-benzyl-1-thio-β-D-glucohexopyranoside.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06153396
Source datasetuspto-grants-2000_11
ORD IDord-f492a3af2c484225b554db1b7e0ab62d
Source noteuspto-grants-2000_11