HuagongsheHuagongshe Chemistry Print Report · For research reference only
(1,1'-Biphenyl)-4-methanol → 1,1'-Biphenyl, 4-(bromomethyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (1,1'-Biphenyl)-4-methanol | HCID 19186 | — |
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | 1,1'-Biphenyl, 4-(bromomethyl)- | HCID 257716 | 111.8% |
Reaction Steps
To a solution of 4-phenylbenzyl alcohol (1.00 g, 5.43 mmol) in a mixture of diisopropyl ether (10 mL) and chloroform (20 mL) was added phosphorus tribromide (0.98 g, 3.62 mmol) with ice-cooling and the mixture was stirred at room temperature for 1 hour. This reaction mixture was diluted with water and extracted with diisopropyl ether. The organic layer was washed with water and saturated aqueous sodium hydrogen carbonate solution, dried over MgSO4, and filtered. The filtrate was concentrated under reduced pressure and the residue was recrystallized from ethanol-hexane to provide 1.00 g of the title compound. Yield 75%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06248766B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-442a58b08b5e45d8bb558dbdda44ea8c |
| Source note | uspto-grants-2001_06 |