HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 578820Generated: October 25, 2026
3-Bromo-2-chloro-5-methylpyridine → 3-Bromo-2-ethoxy-5-methylpyridine
https://huagongshe.com/reaction/578820
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromo-2-chloro-5-methylpyridine | HCID 285437 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Bromo-2-ethoxy-5-methylpyridine | HCID 22591175 | 72% |
Reaction Steps
To a solution of 3-bromo-2-chloro-5-methylpyridine (4.00 g, 19.37 mmol) in ethanol (100 mL) was added sodium ethoxide (6.59 g, 96.9 mmol) in three portions. The mixture was stirred under nitrogen at 100° C. for 2 days. The reaction was cooled to room temperature, diluted with water and extracted with DCM. The combined organic layers were dried (Na2SO4), and the solvent was removed under reduced pressure. Purification (FCC, SiO2, 20%, EtOAc/hexanes) afforded the title compound (3.00 g, 72%). 1H NMR (400 MHz, DMSO-d6) δ 7.94 (dd, J=0.8, 2.3 Hz, 1H), 7.89-7.82 (m, 1H), 4.31 (q, J=7.0 Hz, 2H), 2.18 (t, J=0.8 Hz, 3H), 1.30 (t, J=7.0 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040692B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-a5a5aff655ce452c83686e53b2305a94 |
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| Source note | uspto-grants-2015_05 |
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