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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660557Generated: November 4, 2026

Dichloromethane → HCID 12795697, compound

https://huagongshe.com/reaction/1660557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantHCID 11303394HCID 11303394—
CatalystTetraethylammonium ChlorideHCID 5946—
SolventAcetonitrileHCID 6342—
ProductHCID 12795697HCID 12795697—

Reaction Steps

An about 1:2 mixture of the α- and β-anomers of 3,4,6-tri-O-acetyl-2-azido-2-deoxy-D-galactopyranosyl nitrate (0.377 g, 1.01 mmole) was dissolved in acetonitrile (6 ml) containing tetraethylammonium chloride (0.924 g, 5.05 mmole) and the solution was left at room temperature for 48 hours. The reaction mixture was diluted with dichloromethane (25 ml), washed with water (25 ml) and dried. Evaporation of the solvent in vacuo left a syrup (0.325 g) which showed doublets with spacings of 9.0 and 3.5 Hz at δ5.15 and 6.20 p.p.m., respectively in the p.m.r. spectrum measured in CDCl3. These signals are assigned to the β-(XXIII) and α-anomers (XXII) for 3,4,6-tri-O-acetyl-2-azido-2-deoxy-D-galactopyranosyl chloride, respectively. Judging from the relative intensities of the signals, the product consisted of a near 10:1 mixture of the α- and β-anomers, (XXII) and (XXIII) respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04308376
Source datasetuspto-grants-1981_12
ORD IDord-a8fe83dfd9704a499c8597fb90f9c75d
Source noteuspto-grants-1981_12