HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 2-(1-Chloroethyl)-1,3-benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-(1,3-Benzothiazol-2-yl)ethan-1-ol | HCID 2830674 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(1-Chloroethyl)-1,3-benzothiazole | HCID 10997958 | — |
Reaction Steps
To a solution of 1-(2-benzothiazolyl)ethanol (2.5 g) prepared according to J. Indian Chem. Soc., 566 (1974) in methylene chloride (50 ml) was added thionyl chloride (3.32 g) and the resulting solution stirred at room temperature for 1 hour. The solution was poured onto ice-water (100 ml) and the organic extract separated. This extract was washed with aqueous bicarbonate (10 ml of a 5% solution) and then with water (50 ml). The methylene chloride layer was dried over anhydrous magnesium sulfate and evaporated to a light yellow oil (2.08 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04939140 |
| Source dataset | uspto-grants-1990_07 |
| ORD ID | ord-b7ea343a2c8946b4a3ba7c2e6a332844 |
| Source note | uspto-grants-1990_07 |