HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297959Generated: November 1, 2026
3,5-Dibromopyridine → 3-Bromo-5-(propan-2-yloxy)pyridine
https://huagongshe.com/reaction/2297959
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,5-Dibromopyridine | HCID 69369 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | Potassium propan-2-olate | HCID 23663646 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 3-Bromo-5-(propan-2-yloxy)pyridine | HCID 10584808 | 71.2% |
Reaction Steps
Potassium metal (6.59 g, 168.84 mmol) was dissolved in dry 2-propanol (60.0 mL) under nitrogen. The resulting potassium isopropoxide was heated with 3,5-dibromopyridine (20.00 g, 84.42 mmol) and copper powder (1 g, 5% by weight of 3,5-dibromopyridine) at 140° C. in a sealed glass tube for 14 h. The reaction mixture was cooled to ambient temperature and extracted with diethyl ether (4×200 mL). The combined ether extracts were dried over sodium sulfate, filtered, and concentrated by rotary evaporation. The resulting crude product was purified by column chromatography over aluminum-oxide, eluting with ethyl acetate-hexane (1:9, v/v). Selected fractions were combined and concentrated by rotary evaporation, producing a pale-yellow oil (12.99 g, 71.2%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06492399B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-4fcc9d24a5f640ca8f19555f215b05fc |
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| Source note | uspto-grants-2002_12 |
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