HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21405Generated: October 26, 2026
Phosphorus tribromide → 4-(2-Bromoethyl)benzonitrile
https://huagongshe.com/reaction/21405
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | 4-(2-Hydroxyethyl)benzonitrile | HCID 2800815 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 4-(2-Bromoethyl)benzonitrile | HCID 12886548 | — |
Reaction Steps
A solution of phosphorus tribromide (5 g) in carbon tetrachloride (10 ml) was added, dropwise, to a solution of 4-cyanophenethyl alcohol (8.06 g) in carbon tetrachloride (60 ml). The mixture was heated under reflux for 4 hours. On cooling to room temperature, the mixture was poured onto ice (200 g). The layers were separated and the organic layer was washed with 10% aqueous sodium carbonate (50 ml) and brine (50 ml), dried (MgSO4) and concentrated in vacuo to give a colourless oil which solidified on standing. The solid was chromatographed on silica eluting with ethyl acetate containing hexane (20%). The fractions containing the less polar (higher Rf) product were combined and concentrated in vacuo to give 4-cyanophenethyl bromide as a yellow oil which solidified on standing, yield 8.9 g. The fractions containing the more polar (lower Rf) product were combined and concentrated in vacuo to give the title compound as a colourless solid, yield 0.47 g, m.p. 152°-153° .
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05422358 |
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| Source dataset | uspto-grants-1995_06 |
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| ORD ID | ord-94cc554d11ba4598bc45790c9073d60b |
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| Source note | uspto-grants-1995_06 |
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