HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762259Generated: November 1, 2026
Hydrofluoric Acid → 2,5-Dichloro-3-fluoropyridine
https://huagongshe.com/reaction/1762259
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrofluoric Acid | HCID 14917 | — |
| Reactant | 3-Amino-2,5-dichloropyridine | HCID 2799999 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2,5-Dichloro-3-fluoropyridine | HCID 10964877 | 88% |
Reaction Steps
A 500 ml polytetrafluoroethylene reactor equipped with stirrer, thermometer and reflux condenser is charged with 120 g of hydrogen fluoride. A solution of 40.7 g (0.25 mol) of 3-amino-2,5-dichloropyridine in 60 ml of dimethyl sulfoxide is added dropwise at a temperature in the range from 0° C. to +10° C. Then 20.7 g (0.3 mol) of sodium nitrite are introduced into this solution at +40° C. The resultant nitrogen is removed from the reactor through the reflux condenser. Gas evolution ceases after 4 hours at +40° C. 150 ml of methylene chloride are added to the reaction mixture which is then poured into ice water. The two-phase mixture is neutralised with concentrated ammonia solution. The organic phase is separated and the aqueous phase is extracted three times with methylene chloride. The combined organic phases are washed with water, dried over sodium sulfate and filtered through silica gel. The solution is separated by distillation, affording 36.5 g (88% of theory) of 2,5-dichloro-3-fluoropyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04831148 |
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| Source dataset | uspto-grants-1989_05 |
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| ORD ID | ord-f4a84abd94f54c0dad955b49b4951c23 |
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| Source note | uspto-grants-1989_05 |
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