HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → (5-Bromopentyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Benzyltriphenylphosphonium bromide | HCID 2734970 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (5-Bromopentyl)benzene | HCID 285561 | 94% |
Reaction Steps
Phenylmethyl-triphenylphosphonium bromide (51 a) (PAA 59). Triphenylphosphine (2.364 g, 9.00 mmol) was added to benzyl bromide (1.348 g, 8.00 mmol) in 35 mL toluene in a 100-mL round-bottom flask. The mixture was heated to reflux under argon and stirred 24 h, then concentrated in vacuo. The resulting white amorphous solid was triturated with ether (3×20 mL) to yield 3.268 g (94%) white powder. 1H NMR (CDCl3, 300 MHz) δ 7.58-7.78 (m, 15H), 7.10-7.26 (m, 5H), 5.34-5.42 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07718600B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-ebc5ced329824d9190c1a8b4ab78847a |
| Source note | uspto-grants-2010_05 |