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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747644Generated: October 29, 2026

N,N,N',N'-Tetramethylethylenediamine → HCID 87781368, compound

https://huagongshe.com/reaction/747644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant2-Chloroethyl vinyl etherHCID 8074—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 87782501HCID 87782501—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 87781368HCID 87781368—

Reaction Conditions

Temperature80 °C

Reaction Steps

4-Hydroxyphenyldi(4-t-butylphenyl)sulfonium perfluorobutanesulfonate salt (28.4 g), potassium carbonate (8.56 g), and N,N,N′,N′-tetramethylethylenediamine (0.50 g) were dissolved in dimethyl sulfoxide (143 g). Chloroethyl vinyl ether (6.30 g) was added to the solution, followed by heating to 80° C. The reaction mixture was stirred for 15 hours and cooled to 30° C. or lower. After removal of solid through filtration, water (220 g) and dichloromethane (113 g) were added to the filtrate, whereby the target substance was extracted to the dichloromethane layer. The organic layer was repeatedly washed with distilled water until the pH of the separated aqueous layer was shifted to 7. The solvent was removed by means of a rotary evaporator, and the formed oily substance was dissolved in acetonitrile (100 g). The acetonitrile layer was washed five times with hexane (85 g). The solvent was removed by means of a rotary evaporator, to thereby yield 24.5 g of a brown oily substance. Through 1H-NMR and ion chromatography, the substance was identified to be 4-vinyloxyethoxyphenyldi(4-t-butylphenyl)sulfonium perfluorobutanesulfonate salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07396960B2
Source datasetuspto-grants-2008_07
ORD IDord-0ef5d57c90774179a9adb9b108e1ffed
Source noteuspto-grants-2008_07