HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzisothiazole → 3-Chloro-1,2-benzisothiazole
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzisothiazole | HCID 9225 | — |
| Edukt | Sulfuryl chloride | HCID 24648 | — |
| Lösungsmittel | Chlorobenzene | HCID 7964 | — |
| Produkt | 3-Chloro-1,2-benzisothiazole | HCID 598190 | 96% |
Reaktionsschritte
In a 300 ml four-necked flask equipped with a stirrer, a thermometer, and a condenser, 100 g of monochlorobenzene was placed in advance, to which 27.0 g (0.2 mol) of 1,2-benzisothiazole was added under nitrogen atmosphere. 32.4 g (0.22 mol) Of sulfuryl chloride was added dropwise thereto while stirring at a temperature of from 70° to 80° C. and allowed to react for 1 hour at the same temperature. After the termination of the reaction, the reaction mixture was subjected to distilling off of the solvent and then to distillation under reduced pressure to give 32.5 g of 3-chloro-1,2-benzisothiazole (boiling point: 116° to 118° C./5 mm Hg, melting point: 38° to 40° C.). The yield was 96% to the 1,2-benzisothiazole.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05856504 |
| Quelldatensatz | uspto-grants-1999_01 |
| ORD ID | ord-c4037742b9154d1288c92c8b72230c83 |
| Quellennotiz | uspto-grants-1999_01 |