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 | 97.6% |
Reaction Steps
First, 25.2 g (101 mmol) of 4-bromobenzyl bromide and 100 mL of acetone were put into a 200 mL conical flask, and 29.1 g (111 mmol) of triphenylphosphine was added thereto. The mixture was stirred for 23 hours at room temperature. After the reaction, a precipitate in the reaction mixture was collected by suction filtration to give 50.5 g of a white powdered solid of (4-bromobenzyl)triphenylphosphoniumbromide (yield: 97.6%). A synthesis scheme (f-1) of (4-bromobenzyl)triphenylphosphoniumbromide is shown below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07758972B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-9939ae71dafc41579eeb90e8c7865fb6 |
| Source note | uspto-grants-2010_07 |