HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880468Generated: October 27, 2026
Bicarbonate Ion → 2-Chloro-4,6-dimethylpyridine
https://huagongshe.com/reaction/880468
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bicarbonate Ion | HCID 769 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | 2-Amino-4,6-dimethylpyridine | HCID 21507 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Chloro-4,6-dimethylpyridine | HCID 12508378 | 38.4% |
Reaction Steps
A mixture of 2-amino-4,6-dimethylpyridine (90 g, 0.736 mol) and sodium chloride (216 g, 3.69 mol) in concentrated hydrochloric acid (720 mL) was cooled to between −15 and −20° C. A solution of sodium nitrite (71.2 g, 1.03 mol) in water (135 mL) was added over 30 min. More sodium chloride (216 g, 3.69 mol) was added and the reaction mixture was allowed to warm to ambient temperature and stirred for 1 h. The reaction mixture was basified with solid bicarbonate (700 g) and extracted with dichloromethane (1 L), filtered and the two phases separated. The organic layer was concentrated in vacuo and the crude purified by flash column chromatography over silica gel (100-200 mesh) with 20% dichloromethane in petroleum ether as eluent to afford 2-chloro-4,6-dimethylpyridine (40 g, 38%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08993574B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-954cae20cb8e47b4afe63beaa3c037ca |
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| Source note | uspto-grants-2015_03 |
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