Carbon Dioxide → 2-Fluoro-6-iodo-3-methylbenzoic acid

HRID 1593731Notes

Reaction equation

HRID 1593731 reaction equation
[F:1][C:2]1[CH:7]=[C:6]([I:8])[CH:5]=[CH:4][C:3]=1[CH3:9].[Li+].CC([N-]C(C)C)C.[C:18](=[O:20])=[O:19]>C1COCC1>[F:1][C:2]1[C:3]([CH3:9])=[CH:4][CH:5]=[C:6]([I:8])[C:7]=1[C:18]([OH:20])=[O:19]

Participants

5

Conditions

Temperature
-78 °C

Procedure

A −78° C. solution of 2-fluoro-4-iodo-1-methylbenzene (25 g, 105.9 mmol) in THF (200 mL) was treated dropwise with LDA (2M solution in THF, 58.5 mL, 116 mmol), stirred at −78° C. for 1 hour, treated with excess powdered dry ice, stirred at −78° C. for 30 minutes, and warmed to room temperature gradually over about 18 hours. The mixture was concentrated and the residue was partitioned between 4N NaOH and diethyl ether. The aqueous phase was adjusted to pH 2 with 2N HCl and extracted three times with ethyl acetate. The combined extracts were washed with water and brine, dried (MgSO4), filtered, and concentrated to provide 19.4 g (66% yield) of the desired product. MS (ESI(+)) m/e 279 (M+H)+.

Workup

  1. stirringstirred at −78° C. for 30 minutes
  2. temperaturewarmed to room temperature gradually over about 18 hours
  3. concentrationThe mixture was concentrated
  4. customthe residue was partitioned between 4N NaOH and diethyl ether
  5. extractionextracted three times with ethyl acetate
  6. washThe combined extracts were washed with water and brine
  7. dry with materialdried (MgSO4)
  8. filtrationfiltered
  9. concentrationconcentrated

Sources & evidence

ORD record
ord-7fd99cab04f94cfaaefebdeba267c624
Source dataset
uspto-grants-2007_11
Patent number
US07297709B2

Reaction notes

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