HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70523Generated: October 26, 2026
Hydrochloric Acid → 6-Bromo-3-chloro-2-methoxypyridine
https://huagongshe.com/reaction/70523
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 6-Bromo-2-methoxypyridin-3-amine | HCID 10536137 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | Cupric Chloride | HCID 24014 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Bromo-3-chloro-2-methoxypyridine | HCID 58452302 | 85% |
Reaction Steps
A solution of sodium nitrite (7.04 g) in water (10 mL) was added dropwise to a suspension of 6-bromo-2-methoxypyridin-3-amine (10.4 g) in concentrated hydrochloric acid (35 mL) under ice-cooling. After stirring for 10 minutes, the reaction system was added dropwise to a suspension of copper chloride (12.7 g) in concentrated hydrochloric acid (15 mL) under ice-cooling, and the mixture was stirred at 65° C. for one hour and 15 minutes. The reaction solution was poured into water, followed by extraction with ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=9:1→7:3) to give the title compound as a yellow powder (9.69 g, 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822503B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-0b4c2e290aea47d6954e1ee05dd0c359 |
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| Source note | uspto-grants-2014_09 |
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