HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobenzyl alcohol → 1-(Bromomethyl)-4-chlorobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobenzyl alcohol | HCID 13397 | — |
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(Bromomethyl)-4-chlorobenzene | HCID 69329 | — |
Reaction Steps
To a suspension of 4-chlorobenzyl alcohol (14.26 g, 100 mmol) in CH2Cl2 (40 mL) at ambient temperature was added added dropwise a solution of PBr3 in CH2Cl2 (1.0M, 32 mL, 32 mmol). The reaction mixture was stirred for 72 hours at ambient temperature and then was poured slowly onto ice. The layers were separated and the organic phase was dried over MgSO4, filtered, and concentrated in vacuo to give 4-chlorobenzyl bromide (19.76 g) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05616596 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-b84de76bff364798be1a6cb094b81efd |
| Source note | uspto-grants-1997_04 |