HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 1-(2-Bromoethyl)-4-methoxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Methoxyphenethyl alcohol | HCID 69705 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2-Bromoethyl)-4-methoxybenzene | HCID 84427 | 71.2% |
Reaction Steps
4-Methoxyphenethyl alcohol (50 g) and triphenylphosphine (103 g) were dissolved in methylene chloride (600 ml), followed by the addition of N-bromosuccinimide (70 g) in small portions under ice-cooling, and the resulting mixture was stirred at room temperature for 30 min. The reaction mixture was evaporated, and to the resulting residue was added hexane. The insoluble matters were filtered off, while the resulting filtrate was evaporated, to give the title compound as a colorless oil (50.32 g, yield; 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06790844B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-99f99fe7ad5e4042bf426509a87d034a |
| Source note | uspto-grants-2004_09 |