HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343432Generated: October 27, 2026
Isopropanol → 3-Bromo-5-(propan-2-yloxy)pyridine
https://huagongshe.com/reaction/343432
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | 3,5-Dibromopyridine | HCID 69369 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Catalyst | Copper | HCID 23978 | — |
| Product | 3-Bromo-5-(propan-2-yloxy)pyridine | HCID 10584808 | 31.9% |
Reaction Steps
Under a nitrogen atmosphere, 2-propanol (30 mL) was added to potassium (2.4 g, 61.4 mmol) at 0° C., and the mixture was stirred at 0° C. for 30 min. To the resulting solution was added 3,5-dibromopyridine (4.74 g, 20.0 mmol) and copper powder (250 mg, 3.9 mmol). The mixture was heated under reflux under a nitrogen atmosphere for 70 h. Upon cooling to ambient temperature, the mixture was concentrated under high vacuum to a solid, which was diluted with water (200 mL) and extracted with diethyl ether (3×150 mL). The combined ether extracts were dried (Na2SO4), filtered, and concentrated by rotary evaporation to a dark-brown oil (3.71 g). Purification by column chromatography on silica gel, eluting with 10→20% (v/v) diethyl ether in benzene afforded 1.38 g (31.9%) of 3-bromo-5-isopropoxypyridine as a volatile, colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05861423 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-503c048ba54f4a69a22d8ff50c92ee29 |
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| Source note | uspto-grants-1999_01 |
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