HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylenediamine → 4-Cyano-2'-nitrodiphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4'-Bromo-2-nitrobiphenyl | HCID 21857647 | — |
| Reactant | HCID 178418260 | HCID 178418260 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Cyano-2'-nitrodiphenyl | HCID 11851114 | — |
Reaction Steps
20 g (7.19 10-2 moles) of 4 nitro 4'bromobiphenyl, 11.6 of copper cyanide and 120 ml of DMF are placed in a 250 ml receptacle with a magnetic agitator. The mixture is refluxed for 5 h 30. It is then allowed to cool, acetone is added and the reaction medium is poured into 2 liters of water containing 2 g of ethylene diamine. A precipitate is formed. The solid is filtered out then washed in water and hexane. This raw product is redissolved in chloroform. The organic phase is dried on MgSO4, filtered and evaporated till dry. The solid obtained is recrystallized in an ethanol-chloroform mixture. This provides 13.16 g of product, yield ρ=81.7%, melting point=195° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05264512 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-1ad01d141bc0437d83f2cc676e142a63 |
| Source note | uspto-grants-1993_11 |