HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → [(4-Bromophenyl)methyl]triphenylphosphanium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | [(4-Bromophenyl)methyl]triphenylphosphanium bromide | HCID 2724858 | 195.2% |
Reaction Steps
25.2 g (101 mmol) of 4-bromobenzylbromide and 100 mL of acetone were put into a 200 mL conical flask, and then 29.1 g (111 mmol) of triphenylphosphine was added thereto. Thereafter, this mixture was stirred at room temperature for 23 hours to be reacted. After the reaction, a precipitate in the reaction mixture was collected by suction filtration. Then, 50.5 g of objective 4-bromobenzyltriphenylphosphonium bromide was obtained as a white powdered solid in a yield of 98%. Synthetic scheme of 4-bromobenzyltriphenylphosphonium bromide is illustrated below (synthetic scheme a-1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07935854B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-1db5801c742940349b26226d8b8d0ab0 |
| Source note | uspto-grants-2011_05 |