HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265790Generated: November 1, 2026
N,N,N',N'-Tetramethylethylenediamine → HCID 87572956, compound
https://huagongshe.com/reaction/2265790
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 87574721 | HCID 87574721 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 87572956 | HCID 87572956 | — |
Reaction Steps
4-Hydroxyphenyldi(4-t-butylphenyl)sulfonium 2-trifluoromethylbenzenesulfonate (4.51 g), potassium carbonate (5.30 g), and N,N,N′,N′-tetramethylethylenediamine (0.53 g) were dissolved in dimethyl sulfoxide (30 g). Subsequently, chloroethyl vinyl ether (10.03 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 (150 g) and dichloromethane (93 g) were added to the filtrate 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 8.57 g of a red powdery substance. Through 1H-NMR analysis and ion chromatography, this substance was identified to be 4-vinyloxyethoxyphenyldi(4-t-butylphenyl)sulfonium 2-trifluoromethylbenzenesulfonate.
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-d2d9fcfcee434bbbbddd6a8295316cbd |
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| Source note | uspto-grants-2010_12 |
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