HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 2-(4-Bromophenethyl)-benzyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 2-(4-Bromophenethyl)-benzyl alcohol | HCID 54337302 | — |
| Product | 2-(4-Bromophenethyl)-benzyl bromide | HCID 21502881 | — |
Reaction Steps
A suspension of 28.5 g. (0.098 mole) of 2-(4-bromophenethyl)-benzyl alcohol in 150 ml. of 48% hydrobromic acid is stirred at reflux for 3 hours. The cooled two-phase mixture is extracted with benzene. Evaporation of the washed and dried benzene extract under reduced pressure leaves the product as the residual solid, m.p. 63°-75° C. Recrystallization from hexane affords purified material, m.p. 76°-77.5° C. A sample for analysis melts at 76.5°-78° C. after further recrystallization from hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03988454 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-73b9c40b456d4eeaae413c939f083d61 |
| Source note | uspto-grants-1976_10 |