Imidazole → 3-Hydroxybenzoic Acid

HRID 990603Notes

Reaction equation

HRID 990603 reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][CH:11]=1)[C:5]([O:7]C)=[O:6].C([Si](Cl)(C)C)(C)(C)C.N1C=CN=C1>CN(C)C=O>[OH:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][CH:11]=1)[C:5]([OH:7])=[O:6]

Participants

5

Procedure

Into a 250 mL round bottom flask was added 50 mL of dry dimethyl formamide. Ffifteen parts of the hydroxy benzoate (27) and seventeen parts of tert-butyldimethyl silyl chloride were added to the reaction flask with stirring. Seventeen parts of Imidazole was added in portions and stirring was continued for 10 hours. The reaction mixture was extracted with (3×300 mL) of hexane and the hexane layer was washed twice with 250 mL of water. The organic layer was dried on anhydrous sodium sulfate and the solvent was evaporated under reduced pressure to give an oil, yield 26 parts. This material was pure enough for the next step of the reaction. The material was prepared according to the following equation:

Workup

  1. stirringstirring
  2. extractionThe reaction mixture was extracted with (3×300 mL) of hexane
  3. washthe hexane layer was washed twice with 250 mL of water
  4. dry with materialThe organic layer was dried on anhydrous sodium sulfate
  5. customthe solvent was evaporated under reduced pressure
  6. customto give an oil

Sources & evidence

ORD record
ord-c239ddb111a848f98484dd02ef534514
Source dataset
uspto-grants-2002_10
Patent number
US06461876B1

Reaction notes

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