HuagongsheHuagongshe Chemistry Print Report · For research reference only
4,4'-Dihydroxybiphenyl → HCID 54552651, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4,4'-Dihydroxybiphenyl | HCID 7112 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Homoallyl bromide | HCID 21241 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54552651 | HCID 54552651 | 12% |
Reaction Steps
A solution containing 4,4'-Dihydroxybiphenyl (5 g,26.75 mmol), KOH (1.65 g, 29.5 mmol) and methanol (50 ml) was refluxed for 2 hours. 4-Bromo-1-butene (3.975 g, 29.5 mmol) in methanol (10 ml) was added dropwise over a period of 2 hours to the refluxing reaction mixture. The refluxation was continued for 24 hours. The solvent was then removed. The product was then extracted by dichloromethane (50 ml) and dichloromethane was then removed. The resulting solid was washed with 10% potassium hydroxide solution (17 ml), filtered and recrystallized from ethanol: water (1.1 v/v) mixture. Yield 12%, m.p. 155-157° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05900145 |
| Source dataset | uspto-grants-1999_05 |
| ORD ID | ord-e199c36e9faf47ca8f90fb9f96ad3827 |
| Source note | uspto-grants-1999_05 |