HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfur Dioxide → HCID 15560951, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfur Dioxide | HCID 1119 | — |
| Reactant | 1-(3-Amino-4-bromophenyl)ethan-1-one | HCID 608294 | — |
| Reactant | Chloride dihydrate | HCID 21226388 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15560951 | HCID 15560951 | — |
Reaction Steps
5.35 g of 3'-amino-4'-bromoacetophenone, melting point: 113° C., were diazotized in 50 ml of semi-concentrated hydrochloric acid with 1.75 g of sodium nitrite at 0°-5° C. and then decomposed according to Meerwein with 62 ml of sulfur-dioxide-saturated glacial acetic acid solution and 2 g of copper-II-chloride-dihydrate. chloride-dihydrate. After the addition of 62 ml of water, the 4'-bromo-3'-chlorosulfonylacetophenone was obtained which melted at 107° C. and could be introduced without further purification into about 50 ml of liquid ammonia. After evaporation of the ammonia and treatment with water, 4'-bromo-3'-sulfamoylacetophenone were obtained which melted at 161° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04125614 |
| Source dataset | uspto-grants-1978_11 |
| ORD ID | ord-0c7f9db6e5424eaf9d07c329bc16c747 |
| Source note | uspto-grants-1978_11 |