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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265788Generated: October 30, 2026

N,N,N',N'-Tetramethylethylenediamine → HCID 87574174, compound

https://huagongshe.com/reaction/2265788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant2-Chloroethyl vinyl etherHCID 8074—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 87573466HCID 87573466—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 87574174HCID 87574174—

Reaction Conditions

Temperature80 °C

Reaction Steps

4-Hydroxyphenyldiphenylsulfonium 2,4,6-triisopropylbenzenesulfonate (8.00 g), potassium carbonate (2.46 g), and N,N,N′,N′-tetramethylethylenediamine (0.16 g) were dissolved in dimethyl sulfoxide (24.00 g). Subsequently, chloroethyl vinyl ether (1.59 g) was added to the resultant solution, followed by heating to 80° C. and stirring for 15 hours. The resultant reaction mixture was cooled to 30° C. or lower. After removal of solid matter through filtration, water (160 g) and dichloromethane (64 g) were added to the filtrate for extraction of a target substance into the dichloromethane layer. The organic layer was repeatedly washed with distilled water until the pH of the separated aqueous layer became 7. The solvent was removed by means of a rotary evaporator, and the thus-obtained oily substance was dissolved in acetonitrile (32 g). The acetonitrile layer was washed five times with hexane (24 g). The solvent was removed by means of a rotary evaporator, to thereby yield 9.84 g of a brown oily substance. Through 1H-NMR analysis and ion chromatography, this substance was identified to be 4-vinyloxyethoxyphenyldiphenylsulfonium 2,4,6-triisopropylbenzenesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858287B2
Source datasetuspto-grants-2010_12
ORD IDord-97f7066857b94e8090fe282d69fac77b
Source noteuspto-grants-2010_12