Hydrochloric Acid → HCID 22268744, compound

HRID 488944Notes

Reaction equation

HRID 488944 reaction equation
FC(F)(F)[C:3]([NH:5][C:6]1[CH:7]=[C:8]([CH:13]=[C:14]([C:16]([F:19])([F:18])[F:17])[CH:15]=1)[C:9]([O:11]C)=[O:10])=O.C[Si]([N-][Si](C)(C)C)(C)C.[K+].IC.[OH-].[Li+].Cl>C1COCC1>[CH3:3][NH:5][C:6]1[CH:7]=[C:8]([CH:13]=[C:14]([C:16]([F:17])([F:18])[F:19])[CH:15]=1)[C:9]([OH:11])=[O:10]

Participants

7

Procedure

Methyl 3-(trifluoromethylcarbonyl)amino-5-(trifluoromethyl)benzoate (cf. procedures (116a) and (80a); 131 mg, 0.42 mmol) was dissolved in THF (5 mL), and the resultant solution was charged successively with KHMDS (0.83 mL of a 0.5 M solution) and iodomethane (0.03 mL, 0.42 mL). The mixture was stirred for 16 h, quenched with sat. NaHCO3, and extracted with EtOAc (2×). The organic extracts were combined, washed with brine, dried (Na2SO4), filtered, and concentrated in vacuo. This product was dissolved in 3:1:1 THF/MeOH/water (5 mL) and the resultant solution was charged with lithium hydroxide (20 mg, 0.84 mmol). The reaction was stirred for 14 h, acidified with 1N HCl, and extracted with EtOAc (2×). The organic extracts were combined, washed with water, washed with brine, dried (Na2SO4), filtered, and concentrated in vacuo to provide 3-methylamino-5-(trifluoromethyl)benzoic acid.

Workup

  1. customquenched with sat. NaHCO3
  2. extractionextracted with EtOAc (2×)
  3. washwashed with brine
  4. dry with materialdried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. dissolutionThis product was dissolved in 3:1:1 THF/MeOH/water (5 mL)
  8. stirringThe reaction was stirred for 14 h
  9. extractionextracted with EtOAc (2×)
  10. washwashed with water
  11. washwashed with brine
  12. dry with materialdried (Na2SO4)
  13. filtrationfiltered
  14. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-9e7376272f874e23a6ac2a8882fe7e0a
Source dataset
uspto-grants-2005_12
Patent number
US06974836B2

Reaction notes

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