Methane → 1-(4-Fluorophenyl)-1H-imidazole-4-carboxylic acid

HRID 2055633Notes

Reaction equation

HRID 2055633 reaction equation
C([O:3][C:4]([C:6]1[N:7]=[CH:8][N:9]([C:11]2[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=2)[CH:10]=1)=[O:5])C.C>O1CCOCC1.[OH-].[Na+]>[F:17][C:14]1[CH:13]=[CH:12][C:11]([N:9]2[CH:10]=[C:6]([C:4]([OH:5])=[O:3])[N:7]=[CH:8]2)=[CH:16][CH:15]=1

Participants

5

Reactant 2

HCID 297MethaneHCID 17390092HCID 17390092, compound

Product 1

HCID 173900481-(4-Fluorophenyl)-1H-imidazole-4-carboxylic acid

Reagents, catalysts & solvents 2

HCID 14798Sodium HydroxideSolventHCID 312751,4-DioxaneSolvent

Procedure

Crude 1-(4-fluoro-phenyl)-1H-imidazole-4-carboxylic acid ethyl ester (175 mmol) was dissolved in 450 mL dioxane and 450 mL 2N sodium hydroxide solution. The reaction mixture was refluxed for 2 h. Charcoal (1 g, Norit SA II) was added and reflux was continued for another 20 min. The mixture was filtered hot and washed with 50 mL 2N sodium hydroxide solution. The filtrate was treated with 550 mL 2N HCl and stirred at room temperature overnight. The solid material was filtered off and dried at 50° C. and 15 mbar. The desired compound was obtained as an off-white solid (28 g, 78%), MS: m/e 205.1 (M−H).

Workup

  1. temperatureThe reaction mixture was refluxed for 2 h
  2. temperaturereflux
  3. filtrationThe mixture was filtered hot
  4. washwashed with 50 mL 2N sodium hydroxide solution
  5. additionThe filtrate was treated with 550 mL 2N HCl
  6. filtrationThe solid material was filtered off
  7. customdried at 50° C.

Sources & evidence

ORD record
ord-061f34ee70e24d748c5ff7ae6756faec
Source dataset
uspto-grants-2008_02
Patent number
US07332510B2

Reaction notes

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