Hydrochloric Acid → HCID 17862261, compound

HRID 1610439Notes

Reaction equation

HRID 1610439 reaction equation
[Cl:1][C:2]1[N:7]=[CH:6][C:5]([CH:8]([OH:26])[CH:9]([CH2:15][C:16]2[CH:21]=[CH:20][C:19]([C:22]([F:25])([F:24])[F:23])=[CH:18][CH:17]=2)[C:10]([O:12]CC)=[O:11])=[CH:4][CH:3]=1.[OH-].[Na+].Cl.C(=O)([O-])O.[Na+]>CO>[Cl:1][C:2]1[N:7]=[CH:6][C:5]([CH:8]([OH:26])[CH:9]([CH2:15][C:16]2[CH:21]=[CH:20][C:19]([C:22]([F:23])([F:24])[F:25])=[CH:18][CH:17]=2)[C:10]([OH:12])=[O:11])=[CH:4][CH:3]=1

Participants

6

Procedure

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%).

Workup

  1. additionwas added
  2. extractionThe mixture was extracted with ethyl acetate (200 ml×2)
  3. washThe extract was washed with water and saturated brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customevaporated under reduced pressure
  6. customThe residue was recrystallized from diisopropyl ether-hexane

Sources & evidence

ORD record
ord-c2bfd40155f949b2818bd4ea9655b726
Source dataset
uspto-grants-2006_01
Patent number
US06982348B2

Reaction notes

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