HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267594Generated: November 1, 2026
Dabco → 2-Trifluoromethylvinyl 4-aminophenyl sulfone
https://huagongshe.com/reaction/267594
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dabco | HCID 9237 | — |
| Reactant | 3,3,3-Trifluoropropene | HCID 12672 | — |
| Reactant | 4-Acetamidobenzenesulfonyl iodide | HCID 21555199 | — |
| Reactant | Ethyl chlorophosphate | HCID 86592542 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-Trifluoromethylvinyl 4-aminophenyl sulfone | HCID 53712671 | — |
Reaction Steps
2-trifluoromethylvinyl 4-aminophenyl sulfone is prepared by the addition of 4-acetamidobenzenesulfonyl iodide to 1,1,1-trifluoropropene followed by dehydrohalogenation and removal of the N-acetyl protective group by hydrolysis in a hydrochloric acid-ethanol mixture. The product is dissolved in acetone (25.1 g or 0.1 mol), an acetone solution of 0.1 mol (17.3 g) of ethylphosphorochloridate in acetone added, followed by 11.2 g of 1,4-diazabicyclo[2.2.2]octane in 10% acetone solution. The reaction mixture is stirred for one hour at room temperature, filtered, most of the acetone evaporated, and the residue is mixed with chloroform, washed and worked up. There is thus obtained 4-diethoxyphosphoramidophenyl 2-trifluoromethylvinyl sulfone: ##SPC59##
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-a5433ac917ed4d9a80f1c4a6191edc52 |
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| Source note | uspto-grants-1976_03 |
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