HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetonitrile → [(3,4-Dichlorophenyl)sulfanyl]acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3,4-Dichlorobenzenethiol | HCID 79964 | — |
| Solvent | Water | HCID 962 | — |
| Product | [(3,4-Dichlorophenyl)sulfanyl]acetonitrile | HCID 18542995 | — |
Reaction Steps
17.9 g (0.10 mol) of 3,4-dichlorobenzenethiol are mixed in the cold with a solution of 4.1 g of sodium hydroxide (about 0.1 mol) in 50 ml of water. The mixture is heated to 60°-70° C. and 7.5 ml (0.12 mol; 20% excess relative to the 3,4-dichlorobenzenethiol) of chloroacetonitrile are added dropwise. The whole is then heated under reflux for about 30 minutes and cooled, the oil which has formed is extracted with ether, the ether solution is washed with dilute sodium hydroxide solution and water, until the pH of the wash waters is neutral, and dried over SO4Mg, the SO4Mg is filtered off, the ether is evaporated off and the expected nitrile, which is in the form of a chromatographically pure oil, is collected.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04271194 |
| Source dataset | uspto-grants-1981_06 |
| ORD ID | ord-837cb09b4ae54e5ea14ff08ca4b47179 |
| Source note | uspto-grants-1981_06 |