HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066838Generated: November 1, 2026
Carbon tetrabromide → 4-Bromo-2-(bromomethyl)-1-fluorobenzene
https://huagongshe.com/reaction/1066838
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | (5-Bromo-2-fluorophenyl)methanol | HCID 2773352 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-Bromo-2-(bromomethyl)-1-fluorobenzene | HCID 13553295 | 76% |
Reaction Steps
In a 250 ml round bottom flask, under a nitrogen atmosphere, 2-fluoro-5-bromobenzyl alcohol (5.85 g, 28.5 mmol) was dissolved in diethy ether (125 ml). To this solution triphenylphosphine (9.73 g, 37.1 mmol) and carbon tetrabromide (12.30 g, 37.1 mmol) were added. The resulting mixture was stirred at ambient temperature for about three hours. The progress of the reaction was monitored by thin layer chromatography. The mixture was then stirred at ambient temperature for about 19 additional hours. The reaction mixture was filtered and washed with cold diethyl ether. The filtrate was evaporated, yielding a light yellow oil. The oil was further purified by chromatography on a silica gel with hexanes. The desired fractions were purified by evaporation to yield 5.8 grams of the desired title intermediate. The material slowly crystallized upon standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06245761B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-6106027def1f48f59d1de82d9f8cf9a6 |
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| Source note | uspto-grants-2001_06 |
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