HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → Bromo-4'-chloro-3'-sulfamoylacetophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 5-Acetyl-2-chlorobenzene-1-sulfonamide | HCID 12619798 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Bromo-4'-chloro-3'-sulfamoylacetophenone | HCID 12952390 | — |
Reaction Steps
4.7 g. of 4'-chloro-3'-sulfamoylacetophenone were suspended in 50 ml of ethyl acetate and to that suspension, some drops of a solution of 3.2 g of bromine were added until the mixture was distinctly brown. The suspension was heated to about 60° - 70° C until the color changed (addition of a drop of 48% hydrobromic acid possible), cooled and the residual amount of the bromine solution was added dropwise at room temperature, while stirring. After distilling off the solvent, 2-bromo-4'-chloro-3'-sulfamoylacetophenone was obtained which melted at 169° C (from n-butanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04061761 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-a22a8f8c63544bef8cdc6f6d728e5041 |
| Source note | uspto-grants-1977_12 |