HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetonitrile → 2-(2-Benzothiazolylthio)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178418395 | HCID 178418395 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-Benzothiazolylthio)acetonitrile | HCID 1800033 | — |
Reaction Steps
In a 1 liter flask were combined 33.4 g. (0.2 mole) of 2-mercaptobenzothiazole and 22.4 g. (0.2 mole) of potassium t-butoxide with 300 ml. of tetrahydrofuran. The reaction mass was stirred at room temperature for 15 minutes. Chloroacetonitrile, 16 g. (0.2 mole) was added and the resulting mixture was stirred at room temperature for 1 hour. The mixture was then poured into 400 ml. of benzene and was washed with three 250 ml. portions of water. The benzene phase was dried with anhydrous magnesium sulfate. The solvent was evaporated. There was obtained a yield of 37.2 g. of the title compound, m.p. 75°-77° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04006154 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-c21af86ae2c94abf88a9c0f703b78093 |
| Source note | uspto-grants-1977_02 |