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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265786Generated: October 30, 2026

N,N,N',N'-Tetramethylethylenediamine → HCID 178467770, compound

https://huagongshe.com/reaction/2265786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 22481373HCID 22481373—
Reactant8-Chlorooctyl vinyl etherHCID 56608870—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 178467770HCID 178467770—

Reaction Conditions

Temperature80 °C

Reaction Steps

4-Hydroxyphenyldiphenylsulfonium perfluorobutanesulfonate (2.67 g), potassium carbonate (0.78 g), and N,N,N′,N′-tetramethylethylenediamine (0.05 g) were dissolved in dimethyl sulfoxide (13.3 g). Subsequently, 8-chlorooctyl vinyl ether (1.05 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 (13.3 g) was added to the filtrate, and the aqueous layer was washed thrice with hexane (7.96 g). Dichloromethane (10.6 g) and water (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 2.53 g of a brown oily substance. Through 1H-NMR analysis and ion chromatography, this substance was identified to be 4-vinyloxyoctoxyphenyldiphenylsulfonium perfluorobutanesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858287B2
Source datasetuspto-grants-2010_12
ORD IDord-4a6e3143517e49bbae05ababcc3b2cc6
Source noteuspto-grants-2010_12