HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxybiphenyl → HCID 15675493, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxybiphenyl | HCID 7103 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Heptanenitrile, 7-bromo- | HCID 88737 | — |
| Reactant | HCID 15675492 | HCID 15675492 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Methanol--water (1/1) | HCID 22242641 | — |
| Product | HCID 15675493 | HCID 15675493 | 97% |
Reaction Steps
By the method of Example 34, 7-([1,1'-biphenyl]-4-yloxy)-heptanenitrile was prepared from 7-bromoheptanenitrile and 4-phenylphenol, as shiny flakes from water-methanol, mp 78°-79° C. This material (3.0 g, 10.7 mmol) was heated in ethylene glycol (100 g) containing water (33 ml) and NaOH (10 g). After four hours at reflux, during which the nitrile dissolved and a solid formed, the mixture was cooled, diluted with water (400 ml), and acidified with acetic acid (100 ml). The precipitate was collected by filtration, and dried in vacuo to provide 7-([1,1'-biphenyl]-4-yloxy)heptanoic acid as a white solid (3.1 g 97% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05066658 |
| Source dataset | uspto-grants-1991_11 |
| ORD ID | ord-0039760ae81f407b828110c00bac31a9 |
| Source note | uspto-grants-1991_11 |