HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Dichlobentiazox
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Pseudosaccharin chloride | HCID 64783 | — |
| Reactant | (3,4-Dichloroisothiazol-5-yl)methanol | HCID 16723166 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Dichlobentiazox | HCID 17756624 | 82.2% |
Reaction Steps
In 6 ml of acetonitrile were dissolved 0.62 g (3.10 mmol) of 3-chloro-1,2-benzoisothiazole 1,1-dioxide and 0.57 g (3.10 mmol) of the (3,4-dichloroisothiazol-5-yl)methanol. To the resulting solution was dropwise added 0.34 g (3.4 mmol) of triethylamine, followed by stirring at room temperature for 5 hours to give rise to a reaction. After the completion of the reaction, 12 ml of water was added. The resulting crystals were obtained by filtration. The crystals were washed with water and isopropyl alcohol to obtain 0.89 g (yield: 82%) of 3-(3,4-dichloroisothiazol-5-ylmethoxy)-1,2-benzoisothiazole 1,1-dioxide as a colorless powder (melting point: 165 to 167° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07714140B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-87cfdb9d30a44fab894dfce451049edf |
| Source note | uspto-grants-2010_05 |