HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 1-Bromo-4-phenylbutane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Benzenebutanol | HCID 76889 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Bromo-4-phenylbutane | HCID 259668 | 88% |
Reaction Steps
To a solution of 4-phenyl-1-butanol (5.00 g, 33.3 mmol) and CH2Cl2 (250 mL) 15 at 0° C. was added triphenylphosphine (13.1 g, 50.0 mmol) followed by NBS (8.90 g, 50.0 mmol). After stirring at this temperature for 2 h, the mixture was quenched with H2O (50 mL) and extracted with CH2Cl2 (150 mL) The organic layer was washed with brine (40 mL) and dried (Na2SO4). After concentration, the residue was flushed through two quick columns of silica gel using 2% EtOAc/petroleum ether as an eluant to afford 4-phenylbutyl bromide (6.22 g, 88%) as an intermediate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06214877B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-07a332d7642246ffb2735a3d339fa58a |
| Source note | uspto-grants-2001_04 |