HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 1-(3-Bromopropyl)-4-methylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-(4-Methylphenyl)propan-1-ol | HCID 221893 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(3-Bromopropyl)-4-methylbenzene | HCID 14084859 | 84.8% |
Reaction Steps
Compound 13-1 (690 mg) was dissolved in methylene chloride (30 ml), triphenylphosphine (1.33 g) and N-bromosuccinimide (899 mg) were added under ice-cooling, and the mixture was stirred under ice-cooling for 1 hr, and further at room temperature for 3 hr. The reaction mixture was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. Diethyl ether (50 ml) was added, and the precipitated triphenylphosphine oxide was filtered off. The concentrate of the filtrate was purified by silica gel column chromatography (hexane alone) to give the object product (830 mg) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08129361B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-81d07d8e7b5d4ad2a2327e3c4ef4a575 |
| Source note | uspto-grants-2012_03 |