HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271708Generated: October 26, 2026
Hexafluorophosphoric acid → 2-Bromo-5-(4-chloro-phenyl)-3-fluoro-pyridine
https://huagongshe.com/reaction/271708
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexafluorophosphoric acid | HCID 16211447 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 85969704 | HCID 85969704 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Bromo-5-(4-chloro-phenyl)-3-fluoro-pyridine | HCID 85969709 | — |
Reaction Steps
243 mg (3.53 mmol) sodium nitrite in 0.5 mL water are added dropwise at −5° C. to a solution of 1.00 g (3.53 mmol) 2-bromo-5-(4-chloro-phenyl)-pyridin-3-ylamine in 2 mL water and 2.04 mL concentrated HCl. Then at 0° C. 1.56 mL (10.6 mmol) 60% hexafluorophosphoric acid in water are added and the reaction is stirred for a further hour at 0° C. The diazonium salt is suction filtered, washed with cold water, isopropanol and ether and dried overnight in the desiccator at RT and 7 mbar. This is then added batchwise at 90° C. to 50 mL PE (boiling point 100-140° C.). After the reaction solution has cooled the mixture is made alkaline with saturated Na2CO3 solution. The aqueous phase is extracted with EtOAc and the organic phase is washed successively with saturated Na2CO3 solution and water. The organic phase is dried over MgSO4 and the solvent is eliminated i.vac. The purification is carried out by column chromatography on silica gel (PE).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07452911B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-c10b7e04dd6d4e9397bc7e389a310201 |
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| Source note | uspto-grants-2008_11 |
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