HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → alpha-(3,4-Dichlorophenyl)-alpha-(2,6-dichloro-4-nitrophenyl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (3,4-Dichlorophenyl)acetonitrile | HCID 76690 | — |
| Reactant | 2-Bromo-1,3-dichloro-5-nitrobenzene | HCID 9993312 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | alpha-(3,4-Dichlorophenyl)-alpha-(2,6-dichloro-4-nitrophenyl)acetonitrile | HCID 22008581 | 67% |
Reaction Steps
To 150 ml of 20% hydrous DMSO were added 6.15 g of 3,4-dichlorobenzyl cyanide, 8.13 g of 4-bromo-3,5-dichloronitrobenzene and 1.50 g of sodium hydroxide. The reaction was allowed to proceed for one hour at temperatures ranging from 60 to 70° C. After completion of the reaction, DMSO was removed, and the residue was dissolved in 50 ml of toluene. The solution was washed with water, dried and concentrated. To the concentrate was added ethyl alcohol to cause crystallization to afford the titled compound in a yield of 67%, m.p.171-172° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06211178B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-d5d57baf1dee47728c1cadcd99808389 |
| Source note | uspto-grants-2001_04 |