HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethenesulfonyl fluoride → HCID 131717351, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethenesulfonyl fluoride | HCID 69612 | — |
| Reactant | Ethanone, 1-(2-amino-4,5-dimethoxyphenyl)- | HCID 602085 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 131717351 | HCID 131717351 | 85% |
Reaction Steps
To a mixture of 2-amino-4,5-dimethoxyacetophenone (18 g, 92 mmol) in 125 mL of glacial acetic acid was added in one portion ethenesulfonyl fluoride (11.4 g, 0.1 mol) under nitrogen. After stirring for 1 hour at room temperature the resulting yellow mixture was refluxed for 1 hour. The yellow crystalline solid was diluted with an equal volume of ether, filtered, washed with ether, and air dried. There was obtained the title compound (23.7 g, 85% yield) as a yellow solid, mp 142.5°-146.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05112866 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-26e1bba136e142fd86be912ef49dc591 |
| Source note | uspto-grants-1992_05 |