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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848984Generated: October 31, 2026

1,2-Dimethoxyethane → HCID 21183146, compound

https://huagongshe.com/reaction/848984

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantPotassium CarbonateHCID 11430—
ReactantPhenylboronic AcidHCID 66827—
ReactantHCID 21183185HCID 21183185—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 21183146HCID 21183146—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 6.0 g (21 mmol) of 3-chloro-2-iodo(methylthio)benzene, 5.1 g (42 mmol) of phenylboronic acid, 14 g (100 mmol) of potassium carbonate, 80 mL of 1,2-dimethoxyethane, and 75 mL of water was prepared and deaerated with a stream of nitrogen. Tetrakis(triphenylphosphine)palladium(0) (730 mg, 0.63 mmol) was added and the mixture was heated at about 100° C. under nitrogen with stirring for about 20 hours. Water and ether were added and the aqueous phase was extracted with more ether. The ether phase and extract were combined, washed with saturated aqueous sodium chloride solution, dried over sodium sulfate, and concentrated by evaporation under reduced pressure and then in a Kugelrohr apparatus at 80° C. under 0.5 mm Hg (67 Pascals) pressure. The liquid residue was chromatographed on silica eluting with an 85:15 mixture of hexane and dichloromethane to obtain 4.3 g (87 percent of theory) of the title compound as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06010981
Source datasetuspto-grants-2000_01
ORD IDord-dfef05f1772444a196af8bb21ec6fb60
Source noteuspto-grants-2000_01