HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 4-Vinylbenzyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | (4-Vinylphenyl)methanol | HCID 2735162 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Vinylbenzyl bromide | HCID 640269 | 33.9% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Bromine (16.4 g, 103 mmol) was slowly added to a solution of triphenylphosphine (28.87 g, 110.1 mmol) in CH2Cl2 (260 mL) at 0° C. After 10 minutes, 4-vinylbenzyl alcohol (12.5 g, 93.3 mmol) was added and the reaction mixture was stirred at 0° C. for 2 h. The reaction mixture was washed with water (1×) followed by brine (1×). The organic solution was dried over MgSO4, filtered, and concentrated in vacuo. The product was triturated with petroleum ether (3×), and the ethereal solution was concentrated in vacuo. The residue was purified by flash chromatography (hexanes) to afford 4-vinyl-benzyl bromide (6.23 g). 1H NMR (400 MHz, CDCl3) δ 7.32–7.45 (m, 4H), 6.72 (dd, 1H), 5.77 (d, 1H), 5.28 (d, 1H), 4.50 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06998423B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-2cbeeb0a1a0b4a35a2f6c88d3615d1e7 |
| Source note | uspto-grants-2006_02 |