HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Ethyl-[1,1'-biphenyl]-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Ethyl[1,1'-biphenyl]-3-carboxamide | HCID 20270662 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Diethylene Glycol | HCID 8117 | — |
| Product | 2-Ethyl-[1,1'-biphenyl]-3-carboxylic acid | HCID 20270637 | 104.5% |
Reaction Steps
A stirred solution of 2-ethyl-[1,1'-biphenyl]-3-carboxamide (2.1 g, 0.0093 mole) and potassium hydroxide (26.3 g, 0.4 mole) in 175 ml of 2-hydroxyethyl ether was heated at 163° for approximately 18 hours. The reaction mixture was cooled and diluted with 150 ml of ice water. The solution was acidified with concentrated hydrochloric acid to form a precipitate. The precipitate was isolated by filtration and dissolved in diethyl ether; the ethereal solution was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated to give 2-ethyl-[1,1'-biphenyl]-3-carboxylic acid (2.2 g) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04402973 |
| Source dataset | uspto-grants-1983_09 |
| ORD ID | ord-a4a228e8b5514a63ab0163463c65cf80 |
| Source note | uspto-grants-1983_09 |