HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 53778394, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Trichloroethylene | HCID 6575 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | HCID 21418355 | HCID 21418355 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 53778394 | HCID 53778394 | — |
Reaction Steps
35 g of 5-chloro-4-chloromethyl-3-p-chlorophenyl-pyrazole are added while stirring and slight cooling at 25° to a mixture of 6.15 g of sodium cyanide in 150 ml of dimethylsulfoxide. Stirring is carried out for 2 to 5 hours at this temperature until the reaction is determinated. The solution is mixed with 200 ml of water and 200 ml of trichloroethylene or benzene. The layers are separated. Washing is carried out with the organic solvent. Drying is carried out with sodium sulfate and the organic phase is purified with Tonsil. By reducing in bulk in vacuo 5-chloro-3-p-chlorophenyl-1-phenyl-pyrazole-4-acetonitrile is obtained with a yield equal to 99 % of the theoretical amount; F 129.5°-130.5° (from acetonitrile).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04042702 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-2d70f7bd55d64b76aacb1694ecf02d13 |
| Source note | uspto-grants-1977_08 |