HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 1-(Benzyloxy)-4-(bromomethyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | (4-(Benzyloxy)phenyl)methanol | HCID 70043 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(Benzyloxy)-4-(bromomethyl)benzene | HCID 10492756 | 92.6% |
Reaction Steps
To 4-benzyloxybenzyl alcohol (8.1 g, 37.8 mmol) in dichloromethane (160 mL) was added N-bromosuccinimide (7.4 g, 41.6 mmol) followed by portionwise addition of triphenylphosphine (10.9 g, 41.6 mmol). The reaction mixture was stirred at room temperature for 5 minutes, and was then concentrated in vacuo. Purification by flash chromatography, eluting with 80:20 hexanes/ethyl acetate, provided 9.7 g (92%) of 1 as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06376524B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-f39884177c904d33a35be9aaa071ab23 |
| Source note | uspto-grants-2002_04 |