Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dabco | HCID 9237 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Benzenesulfonyl fluoride, 3-(chlorosulfonyl)- | HCID 75603 | — |
| Reactant | 2-Cyanovinyl 4-aminophenyl sulfone | HCID 54561326 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 54410119 | HCID 54410119 | — |
Reaction Steps
To an acetone solution of 10.4 g (0.05 mol) 2-cyanovinyl 4-aminophenyl sulfone is added 12.8 g (0.05 mol of 3-fluorosulfonylbenzenesulfonyl chloride at room temperature, with agitation. The sulfonyl chloride dissolves immediately, giving a clear yellow solution. To this mixture is added over a ten minute period an acetone solution of 1,4-diazabicyclo[2.2.2]-octane (11.2 g, 0.05 mol). A light yellow precipitate forms almost at once; the reaction mixture is maintained at about 25° C for 30 minutes with stirring. Precipitation in water and workup affords a bright yellow powder, 2-cyanovinyl 4-(3-fluorosulfonylbenzenesulfonamido)phenyl sulfone: ##SPC44##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03943154 |
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| Source dataset | uspto-grants-1976_03 |
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| ORD ID | ord-a2723df0638d4742995091f7c46cb9f3 |
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| Source note | uspto-grants-1976_03 |
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