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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | 2-Chloroethyl vinyl ether | HCID 8074 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 87782501 | HCID 87782501 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 87781368 | HCID 87781368 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07396960B2 |
|---|
| Source dataset | uspto-grants-2008_07 |
|---|
| ORD ID | ord-0ef5d57c90774179a9adb9b108e1ffed |
|---|
| Source note | uspto-grants-2008_07 |
|---|