Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Ethyl-6-methoxypyridine | HCID 5324777 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178436455 | HCID 178436455 | — |
Reaction Steps
step 3—A mixture of 26 (530 mg), 48% HBr (1.05 mL) and HOAc (10 mL) in a sealed tube was heated at 90° C. overnight. The reaction mixture was cooled to RT, carefully poured into saturated aqueous NaHCO3 solution, and then extracted with EtOAc. The organic layer was washed with brine, dried (Na2SO4) and concentrated to afford 2-ethyl-6-hydroxypyridine (28) as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08273773B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-61277dc162d94979be01d3fe0401a79b |
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| Source note | uspto-grants-2012_09 |
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