HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-(5-pentylpyridin-2-yl)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethylene Glycol | HCID 8117 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 19867194 | HCID 19867194 | — |
| Product | 4-(5-pentylpyridin-2-yl)benzoic acid | HCID 2053671 | — |
Reaction Conditions
| Temperature | 175 °C |
|---|
Reaction Steps
A mixture of 3.026 g of 2-(cyanophenyl)-5-pentylpyridine, 125 ml of diethylene glycol and 13.8 g of potassium hydroxide was heated to 175° C. for 1.5 hours while stirring and gassing with nitrogen. The reaction mixture was then left to cool, adjusted to pH 8 with semi-concentrated hydrochloric acid and extracted with methylene chloride. The organic phase was washed with water, dried over sodium sulphate, filtered and concentrated. The crude p-(5-pentyl-2-pyridyl)benzoic acid obtained was recrystallized from acetone/hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04898455 |
| Source dataset | uspto-grants-1990_02 |
| ORD ID | ord-769311d1227f4266ad3460577a88a9e4 |
| Source note | uspto-grants-1990_02 |