HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 3-Chloro-1,2-benzisothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1,2-Benzisothiazol-3(2H)-one | HCID 17520 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 3-Chloro-1,2-benzisothiazole | HCID 598190 | 90% |
Reaction Steps
A 1 L four-neck flask equipped with a stirrer, a thermometer and a condenser tube was charged with 75.6 g (0.5 mol) of 1,2-benzisothiazol-3-one, 54.8 g (0.75 mol) of N,N-dimethylformamide and 100.0 g of chlorobenzene. While stirring, 71.4 g (0.6 mol) of thionyl chloride was added dropwise thereto over 1 hour at 70° to 80° C., and the mixture was reacted at the same temperature for 8 hours. After terminating the reaction, the liquid reaction mixture was concentrated, and a crude product obtained was distillated under reduced pressure of 0.93 kPa at 128° C. to give 75.1 g (0.45 mol) of 3-chloro-1,2-benzisothiazole. The yield based on the 1,2-benzisothiazol-3-one was 90%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08664404B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-009e201c73bd4121af068eddd04aa4bd |
| Source note | uspto-grants-2014_03 |