HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → 4-[5-(4-Pentylphenyl)pyrimidin-2-YL]benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 4-(5-(4-Pentylphenyl)pyrimidin-2-yl)benzamide | HCID 15564074 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-[5-(4-Pentylphenyl)pyrimidin-2-YL]benzonitrile | HCID 15564083 | — |
Reaction Steps
4.2 g. of 4-[5-(4-n-pentylphenyl)-2-pyrimidyl]-benzoic acid amide are reacted under reflux in a mixture of 200 ml. of ethylene chloride and 2.5 ml. of phosphorus oxychloride for 1 hour, with stirring. The reaction mixture is diluted with ether and washed with 2N sodium hydroxide solution and then with water until neutral. After evaporation of the organic phase, which has been dried over sodium sulfate, 5-(4-n-pentylphenyl)-2-(4-cyanophenyl)-pyrimidine is obtained and is filtered on a short silica gel column and subsequently recrystallized from methylene chloride/methanol, m.p. 125.5°; cl.p. 242.5°-243°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04062798 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-4bb34a08ef3c44eb80b788415e2a0e17 |
| Source note | uspto-grants-1977_12 |