Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 22261661 | HCID 22261661 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 17862261 | HCID 17862261 | 89% |
Reaction Steps
To a solution of ethyl(2RS,3RS)-3-(6-chloro-3-pyridyl)-3-hydroxy-2-((4-(trifluoromethyl)phenyl)methyl)propionate (9.0 g, 23.2 mmol) in methanol (23 ml) was added 2N aqueous sodium hydroxide solution (23.2 ml, 46.4 mmol), and the mixture was stirred overnight at room temperature. The reaction solution was acidified with 1N hydrochloric acid, and saturated aqueous sodium hydrogen carbonate was added to adjust the pH to 8. The mixture was extracted with ethyl acetate (200 ml×2). The extract was washed with water and saturated brine, dried over anhydrous magnesium sulfate and evaporated under reduced pressure. The residue was recrystallized from diisopropyl ether-hexane to give (2RS,3RS)-3-(6-chloro-3-pyridyl)-3-hydroxy-2-((4-(trifluoromethyl)phenyl)methyl)propionic acid (7.4 g, 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06982348B2 |
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| Source dataset | uspto-grants-2006_01 |
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| ORD ID | ord-c2bfd40155f949b2818bd4ea9655b726 |
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| Source note | uspto-grants-2006_01 |
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