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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564897Generated: October 30, 2026

Pyridine → allyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-alpha-D-mannopyranoside

https://huagongshe.com/reaction/564897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDiethyl EtherHCID 3283—
ReactantBoron trifluorideHCID 6356—
ReactantAllyl AlcoholHCID 7858—
ReactantAcetic AnhydrideHCID 7918—
ReactantN-Acetyl-D-MannosamineHCID 439281—
SolventNitromethaneHCID 6375—
Productallyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-alpha-D-mannopyranosideHCID 13968146—

Reaction Steps

A solution of ManNAc (5.0 g, 2.6 mmol), and Ac2O (10 mL) in pyridine (20 mL) was stirred for 10 hours at room temperature, and the mixture was concentrated, followed by coevaporation with toluene. A solution of the residue, allyl alcohol (2.63 g, 45.2 mmol; 3.1 mL), BF3&Circlesolid;OEt2 (1.60 g, 11.3 mmol; 1.39 mL) in CH3NO2 (150 mL) was gently refluxed for 2.5 hours. After cooling, the mixture was concentrated. The residue was chromatographed on silica gel, with toluene-EtOAc (1:2) to give allyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-mannopyranoside in 6.47 g (74 percent);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06168934A
Source datasetuspto-grants-2001_01
ORD IDord-66bddea7bb3f4888bdda52725ed90a81
Source noteuspto-grants-2001_01