HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713006Generated: November 1, 2026
4,6-Dibromo-2-methylpyridin-3-ol → 6-Bromo-2-methylpyridin-3-ol
https://huagongshe.com/reaction/713006
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4,6-Dibromo-2-methylpyridin-3-ol | HCID 11448524 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Bromo-2-methylpyridin-3-ol | HCID 11194787 | 95% |
Reaction Steps
4,6-Dibromo-2-methylpyridin-3-ol (15.8 g, 59.4 mmol) was dissolved in THF (200 mL). The solution was cooled to −78° C. and n-BuLi (50 mL, 125 mmol, 2.5 M in hexane) was added dropwise keeping the temperature below −78° C. The reaction mixture was allowed to stir at that temperature for 2 hours. The reaction mixture was quenched with water (50 mL) and was neutralized with 2 N HCl. The aqueous mixture was extracted with dichloromethane (2 times). The combined organic layers were dried (Na2SO4) and concentrated in vacuo to give 6-bromo-2-methylpyridin-3-ol (10.5 g, 95%) as a yellow oil. 1H-NMR (300 MHz, DMSO) 2.29 (s, 3H), 7.08 (d, 1H), 7.26 (d, 1H), 10.08 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181273B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-643f0682ba7a4f208fb79cd8fbbfdcfd |
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| Source note | uspto-grants-2015_11 |
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