HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetonitrile → [(5-Chloro-1,3-benzothiazol-2-yl)sulfanyl]acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178527796 | HCID 178527796 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | [(5-Chloro-1,3-benzothiazol-2-yl)sulfanyl]acetonitrile | HCID 13312471 | — |
Reaction Steps
51.0 g (0.254 m), 5-chloro-2-mercaptobenzothiazole, 22.8 g (0.304 m) chloroacetonitrile and 30.7 g triethylamine are dissolved in 600 ml of toluene and the solution is heated to reflux for 3 hr, then allowed to cool to room temperature. The toluene solution is washed with water, dried over anhydrous magnesium sulfate and treated with Darco. After the solvent is removed, the residual solid is recrystallized from 300 ml. benzene. The recovered material is recrystallized from cyclohexane. A total yield of 52 g (86%) is obtained. The recrystallized sample has a melting point of 96°-7° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04443606 |
| Source dataset | uspto-grants-1984_04 |
| ORD ID | ord-f11a01adcb744535b2e4d99644d3bd84 |
| Source note | uspto-grants-1984_04 |