Ethyl Acetate → 4-Bromo-2-fluoro-benzoic acid methyl ester

HRID 1045154Notes

Reaction equation

HRID 1045154 reaction equation
[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[C:4]([F:11])[CH:3]=1.[C:12](OCC)(=O)C.C[Si](C=[N+]=[N-])(C)C>CO>[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([O:8][CH3:12])=[O:7])=[C:4]([F:11])[CH:3]=1

Participants

5

Reactant 3

HCID 8857Ethyl AcetateHCID 167693TrimethylsilyldiazomethaneHCID 3026814-Bromo-2-fluorobenzoic acid

Product 1

HCID 113453114-Bromo-2-fluoro-benzoic acid methyl ester

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

4-Bromo-2-fluorobenzoic acid (5.00 g) was added to ethyl acetate (35 mL) and methanol (35 mL). Trimethylsilyldiazomethane (2M solution in diethyl ether, 12.56 mL) was added slowly and the solution was mixed at room temperature for 30 minutes. The solvent was removed under vacuum, and the crude material was dissolved in ethyl acetate. The solution was extracted with 0.5M sodium hydroxide and dried with brine then anhydrous sodium sulfate. After filtration, the solvent was removed under vacuum to afford crude product of sufficient purity for subsequent use.

Workup

  1. additionthe solution was mixed at room temperature for 30 minutes
  2. customThe solvent was removed under vacuum
  3. dissolutionthe crude material was dissolved in ethyl acetate
  4. extractionThe solution was extracted with 0.5M sodium hydroxide
  5. dry with materialdried with brine
  6. filtrationAfter filtration
  7. customthe solvent was removed under vacuum
  8. customto afford crude product of sufficient purity for subsequent use

Sources & evidence

ORD record
ord-69b1b2835ebb4d5aaeb4c42b756104ab
Source dataset
uspto-grants-2013_10
Patent number
US08563735B2

Reaction notes

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