HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → Benzene, 1-(bromomethyl)-3-(phenylmethyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1,2-Dibromo-1,1,2,2-tetrachloroethane | HCID 69426 | — |
| Reactant | 3-Benzylbenzyl alcohol | HCID 597613 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Benzene, 1-(bromomethyl)-3-(phenylmethyl)- | HCID 9992801 | 100.5% |
Reaction Steps
A solution of 3-benzylbenzyl alcohol (1.98 g) in diethyl ether (60 cm3) was cooled in an ice bath, and 1,1,2,2-tetrachloro-1,2-dibromoethane (3.90 g) added. When the addition was complete, triphenyl phosphine (3.14 g) was added to the cooled mixture. The reaction mixture was stirred for 10 minutes, then filtered and the solvent evaporated under reduced pressure. The resultant yellow oil was purified by column chromatography on a silica gel support, eluting with petroleum ether (boiling range 60°-80° C.) containing 10% by volume diethyl ether, to give 3-benzylbenzyl bromide (2.62 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05225607 |
| Source dataset | uspto-grants-1993_07 |
| ORD ID | ord-d28331d7d71145f8847a7e9bd5fcafb3 |
| Source note | uspto-grants-1993_07 |