HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphonium bromide → [2-(2-Chlorobenzyloxy)-5-fluorobenzyl]triphenylphosphonium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphonium bromide | HCID 80811 | — |
| Reactant | 2-(2-Chlorobenzyloxy)-5-fluorobenzyl alcohol | HCID 57864329 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | [2-(2-Chlorobenzyloxy)-5-fluorobenzyl]triphenylphosphonium bromide | HCID 86634289 | — |
Reaction Steps
4.60 g (17 mmol) of 2-(2-chlorobenzyloxy)-5-fluorobenzyl alcohol are dissolved in 10 ml of acetonitrile, then 5.62 g (16 mmol) of triphenylphosphine hydrobromide are added, and the suspension is stirred under reflux for 12 h. A further 2.80 g (8 mmol) of triphenylphosphine hydrobromide are added, and the mixture is stirred under reflux for a further 3 h. The solvent is mostly distilled out in vacuo, the crystals which have separated out are stirred with petroleum ether, filtered off with suction and dried on a clay dish. 9.82 g (15.7 mmol, 92% of theory) of the title compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08173704B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-f099c4c3604a45d9a237cfcf4addd789 |
| Source note | uspto-grants-2012_05 |