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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 907069Generated: October 26, 2026

Toluene → 4-Chloro-2-(5-isoxazolyl)-5-methylphenyl 2,3,4-tri-O-acetyl-5-thio-beta-D-xylopyranoside

https://huagongshe.com/reaction/907069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant4-Chloro-2-(5-isoxazolyl)-5-methylphenolHCID 854042—
Reactant2,3,4-tri-O-acetyl-5-thio-alpha-xylopyranosyl bromideHCID 10926314—
CatalystZincchlorideHCID 3007855—
CatalystSilver imidazolateHCID 10931941—
SolventAcetonitrileHCID 6342—
Product4-Chloro-2-(5-isoxazolyl)-5-methylphenyl 2,3,4-tri-O-acetyl-5-thio-beta-D-xylopyranosideHCID 2483123110%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 0.8 g (5.87 mmol) of zinc chloride, 2 g of 13× molecular sieve, 2 g (5.6 mmol) of 2,3,4-tri-O-acetyl-5-thio-α-D-xylopyranosyl bromide, 1 g (4.77 mmol) of 4-chloro-2-(5-isoxazolyl)-5-methylphenol, 1 g (5.7 mmol) of silver imidazolate, 5 ml of toluene and 5 ml of acetonitrile is prepared. The mixture is kept stirred at 80° C. for 90 minutes and then cooled and filtered. The residual solid is rinsed on the filter with methanol and the combined filtrates are concentrated under reduced pressure. The crude product obtained is purified by chromatography on silica gel, elution being carried out using a dichloromethane/ethyl acetate mixture (9/1; v/v). The pure fraction is crystallized from ethyl ether. The expected compound is thus obtained in the form of a white solid with a yield of 10%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08013010B2
Source datasetuspto-grants-2011_09
ORD IDord-11ee1b2f8c374600a95f8a22fe0cc99f
Source noteuspto-grants-2011_09