HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711513Generated: October 29, 2026
3,5-Dibromopyridine → 3-Bromo-5-(propan-2-yloxy)pyridine
https://huagongshe.com/reaction/1711513
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 crude product obtained 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 | US07790757B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-fc22be19661b496499a57cd3f541c901 |
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| Source note | uspto-grants-2010_09 |
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