HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → Benzonitrile, 4-[5-(4-butylphenyl)-2-pyrimidinyl]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 4-[5-(4-n-Butylphenyl)-2-pyrimidinyl] benzoic acid amide | HCID 15564073 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Benzonitrile, 4-[5-(4-butylphenyl)-2-pyrimidinyl]- | HCID 113397 | — |
Reaction Steps
102.75 G. of 4-[5-(4-n-butylphenyl)-2-pyrimidyl] benzoic acid amide are refluxed for 80 minutes in a mixture of 1500 ml. of ethylene chloride and 34 ml. of phosphorus oxychloride with stirring. The mixture, diluted with ether, is washed with 2-N sodium hydroxide solution and then with water until neutral. After evaporation of the organic phase, which has been dried over sodium sulfate, there is obtained 5-(4-n-butylphenyl)-2-(4-cyanophenyl)pyrimidine which is filtered on a short silica gel column and subsequently recrystallized from methylene chloride/methanol; melting point 94.7° C.; clearing point 246°-246.7° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04180475 |
| Source dataset | uspto-grants-1979_12 |
| ORD ID | ord-30a2fb631f92478e8d0b6796a9561373 |
| Source note | uspto-grants-1979_12 |