Hydrochloric Acid → 6-(2,2,2-Trifluoroethoxy)pyridine-3-carboxylic acid

HRID 341524Notes

Reaction equation

HRID 341524 reaction equation
Cl[C:2]1[N:7]=[CH:6][C:5]([C:8]([OH:10])=[O:9])=[CH:4][CH:3]=1.[F:11][C:12]([F:16])([F:15])[CH2:13][OH:14].[OH-].[K+].Cl>CS(C)=O>[F:11][C:12]([F:16])([F:15])[CH2:13][O:14][C:2]1[N:7]=[CH:6][C:5]([C:8]([OH:10])=[O:9])=[CH:4][CH:3]=1

Participants

6

Procedure

A mixture of 6-chloropyridine-3-carboxylic acid (6.0 g, 38.1 mmol), 2,2,2-trifluoroethanol (8.2 mL, 114.2 mmol) and potassium hydroxide (10.7 g, 190.4 mmol) in DMSO (50 mL) was stirred at 120 C for 18 h and left standing at room temperature for 2 days. A further 2 equivalents of potassium hydroxide and 1.5 equivalent of 2,2,2-trifluoroethanol were added and the reaction mixture was stirred at 120 C for 18 h. The mixture was acidified with a concentrated aqueous solution of HCl until a cream precipitate appeared. The precipitate was collected by filtration, washed with a 1N aqueous solution of HCl before being dissolved in EtOAc, washed 3 times with a 1N aqueous solution of HCl and 3 times with brine. The organic phase was dried over sodium sulfate, filtered and concentrated under vacuum to afford the title compound as a cream solid (6.9 g, 82%). Method C HPLC-MS: MH+ requires m/z=222 Found: m/z=222, Rt=1.24 min (98%).

Workup

  1. waitleft
  2. waitstanding at room temperature for 2 days
  3. stirringthe reaction mixture was stirred at 120 C for 18 h
  4. filtrationThe precipitate was collected by filtration
  5. washwashed with a 1N aqueous solution of HCl
  6. dissolutionbefore being dissolved in EtOAc
  7. washwashed 3 times with a 1N aqueous solution of HCl and 3 times with brine
  8. dry with materialThe organic phase was dried over sodium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated under vacuum

Sources & evidence

ORD record
ord-3acf4d7566d94215bb391f58f29d2d7f
Source dataset
uspto-grants-2014_11
Patent number
US08895733B2

Reaction notes

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