Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-Bromo-4-methylpyridine-2-carboxylic acid | HCID 45790031 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | Ethyl 5-bromo-4-methylpicolinate | HCID 66933529 | — |
Reaction Steps
To a suspension of crude 5-bromo-4-methyl-pyridine-2-carboxylic acid (10.9 g, as potassium salt, approximately 35.5 mmol) in ethanol (120 mL), H2SO4 (0.5 mL) is added. The mixture is stirred at 70° C. for 18 h. The pH of the clear solution is adjusted to pH 9 by adding sat. aq. NaHCO3-solution and the mixture was extracted with diethyl ether (3×300 mL). The combined org. extracts are dried over MgSO4, filtered and concentrated to give 5-bromo-4-methyl-pyridine-2-carboxylic acid ethyl ester (8.20 g) as a green oil; LC-MS: tR=0.87 min, [M+1]+=243.91.
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-d5092a3198c64344946d5cb90a90d372 |
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| Source note | uspto-grants-2013_12 |
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