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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265785Generated: November 1, 2026

N,N,N',N'-Tetramethylethylenediamine → HCID 87574591, compound

https://huagongshe.com/reaction/2265785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant2-Chloroethyl vinyl etherHCID 8074—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 87573325HCID 87573325—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 87574591HCID 87574591—

Reaction Conditions

Temperature80 °C

Reaction Steps

4-Hydroxy-3,5-dimethylphenyldi(4-t-butylphenyl)sulfonium perfluorobutanesulfonate (28.6 g), potassium carbonate (8.10 g), and N,N,N′,N′-tetramethylethylenediamine (0.46 g) were dissolved in dimethyl sulfoxide (142 g). Subsequently, chloroethyl vinyl ether (6.08 g) was added to the resultant solution, followed by heating to 80° C. and stirring for 19 hours. The resultant reaction mixture was cooled to 30° C. or lower. After removal of solid matter through filtration, water (20.9 g) was added to the filtrate, and the aqueous layer was washed thrice with hexane (85.1 g). Dichloromethane (226 g) and water (141 g) were added to the washed aqueous layer, followed by stirring 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, to thereby yield 27.4 g of a brown oily substance. Through 1H-NMR analysis and ion chromatography, this substance was identified to be 4-vinyloxyethoxy-3,5-dimethylphenyldi(4-t-butylphenyl)sulfonium perfluorobutanesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858287B2
Source datasetuspto-grants-2010_12
ORD IDord-09830a89d38d4717acf9f211790ae3d3
Source noteuspto-grants-2010_12