HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908759Generated: October 27, 2026
Isopropanol → 5-Bromo-3-methyl-2-[(propan-2-yl)oxy]pyridine
https://huagongshe.com/reaction/1908759
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | 2,5-Dibromo-3-methylpyridine | HCID 817680 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | 5-Bromo-3-methyl-2-[(propan-2-yl)oxy]pyridine | HCID 22591177 | — |
Reaction Steps
To a solution of potassium tert. butylate (1.26 g, 11.3 mmol) in isopropanol (30 mL), 2,5-dibromo-3-picoline (2.89 g, 11.3 mmol) is added. The mixture is stirred at 80° C. for 15 h before another portion of potassium tert.-butylate (2.53 g, 27.5 mmol) is added. Stirring is continued at 80° C. for 24 h before the mixture is diluted with sat. aq. NaHCO3-solution. The mixture is extracted with ether, the org. extract is dried over MgSO4, filtered and concentrated. The crude product is purified by CC on silica gel eluting with heptane:EA 9:1 to give 5-bromo-2-isopropoxy-3-methyl-pyridine (1.24 g) as a colourless oil; LC-MS: tR=1.06 min; [M+1]+=230.00; 1H NMR (CDCl3): δ 1.35 (d, J=6.3 Hz, 6H), 2.16 (s, 3H), 5.27 (hept, J=6.3 Hz, 1H), 7.48 (d, J=1.5 Hz, 1H), 8.02 (d, J=2.0 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598208B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-7a182ca673d2437883438d224b3682a1 |
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| Source note | uspto-grants-2013_12 |
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