Methanol → Methyl 3-amino-4-fluorobenzoate

HRID 2045497Notes

Reaction equation

HRID 2045497 reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[F:11])[C:5]([OH:7])=[O:6].S(Cl)(Cl)=O.[CH3:16]O>>[CH3:16][O:6][C:5](=[O:7])[C:4]1[CH:8]=[CH:9][C:10]([F:11])=[C:2]([NH2:1])[CH:3]=1

Participants

4

Procedure

To a stirred solution of 3-amino-4-fluoro-benzoic acid (25 g, 161 mmol) in methanol (300 mL) was added thionyl chloride (30 mL, 403 mmol) dropwise at 0° C. Then the mixture solution was refluxed for 12 hours before cooling to room temperature. Then the reaction mixture was concentrated in vacuo and the residue was dissolved in ethyl acetate (500 mL), washed with saturated aqueous sodium bicarbonate solution (3×100 mL), dried over anhydrous sodium sulfate and concentrated in vacuo to afford 3-amino-4-fluoro-benzoic acid methyl ester (27.5 g, quant.) as a pale-white solid: LC/MS m/e calcd for C8H8FNO2 (M+H)+: 170.16, observed: 169.9.

Workup

  1. temperatureThen the mixture solution was refluxed for 12 hours
  2. concentrationThen the reaction mixture was concentrated in vacuo
  3. dissolutionthe residue was dissolved in ethyl acetate (500 mL)
  4. washwashed with saturated aqueous sodium bicarbonate solution (3×100 mL)
  5. dry with materialdried over anhydrous sodium sulfate
  6. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-119508f4649146f8bfa5dca208445827
Source dataset
uspto-grants-2013_11
Patent number
US08586747B2

Reaction notes

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