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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993728Generated: October 30, 2026

1,2-Dimethoxyethane → HCID 68897965, compound

https://huagongshe.com/reaction/1993728

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 68899570HCID 68899570—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
ProductHCID 68897965HCID 6889796542%

Reaction Conditions

Temperature120 °C

Reaction Steps

A solution of 0.108 g (1.02 mM) of sodium carbonate in 2 ml of water, 0.055 g (0.0678 mM) of [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II) dichloromethane and 0.277 g (1.35 mM) of 4,4,5,5-tetramethyl-2-phenyl-1,2,3-dioxaborolane are added to a solution of 0.31 g (0.678 mM) of 2-chloromethylimidazo[1,2-α]pyridin-8-yl 2,3,4-tri-O-acetyl-5-thio-D-xylopyranoside obtained according to example 31, in 4 ml of DME. The reaction mixture is microwave-heated at 120° C. for 30 minutes. After cooling, water is added and the resulting mixture is extracted with ethyl acetate. The organic phase is dried over sodium sulfate and is concentrated under reduced pressure. The evaporation residue is purified by silica gel chromatography, elution being carried out with a dichloromethane/methanol mixture (97/3; v/v), and then crystallized from ether. The expected product is obtained in the form of a white solid with a yield of 42%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652032B2
Source datasetuspto-grants-2010_01
ORD IDord-f2b8395fbd3d46b0af323c9e2b0a8f1c
Source noteuspto-grants-2010_01