HuagongsheHuagongshe Chemistry Print Report · For research reference only
4,4'-Dihydroxybiphenyl → 4,4'-Dibutoxybiphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4,4'-Dihydroxybiphenyl | HCID 7112 | — |
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 131725261 | HCID 131725261 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4,4'-Dibutoxybiphenyl | HCID 604312 | — |
Reaction Steps
In the same manner as in (1) above, 4,4′-dihydroxybiphenyl, 1-bromobutane and potassium carbonate were reacted in a proportion of 1:6:6 to prepare the objective compound. The reaction was conducted by heating under reflux at the refluxing temperature of acetone for 6 hours. The reaction solution thus obtained was cooled, potassium carbonate was filtered off, the filtrate was concentrated under reduced pressure and put into water, and the precipitate thus formed was collected by filtration and recrystallized from ethanol to obtain 4,4′-dibutoxybiphenyl.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07279244B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-256ac2f377584d2b86d3a0d9ca41f95f |
| Source note | uspto-grants-2007_10 |