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
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 87573325 | HCID 87573325 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 87574591 | HCID 87574591 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07858287B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-09830a89d38d4717acf9f211790ae3d3 |
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| Source note | uspto-grants-2010_12 |
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