2-Bromophenylacetic acid → Methyl 2-(2-bromophenyl)acetate

HRID 1408782Notes

Reaction equation

HRID 1408782 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][C:9]([OH:11])=[O:10].O.[CH3:13]C1C=CC(S(O)(=O)=O)=CC=1>CO>[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][C:9]([O:11][CH3:13])=[O:10]

Participants

4

Procedure

To a solution of 2-(2-bromophenyl)acetic acid (2 g, 9.3 mmol) in anhydrous methanol (20 mL) was added 4-methylbenzenesulfonic acid hydrate (1.767 g, 9.3 mmol). The mixture was heated to reflux for 3 hr. The solvent was removed in vacuum. Ethyl ether and water was added. The organic phase was washed with water and brine, then dried over Na2SO4, filtered and concentrated to give methyl 2-(2-bromophenyl)acetate (2 g, 80%), which was used for next step without purification.

Workup

  1. temperatureThe mixture was heated
  2. temperatureto reflux for 3 hr
  3. customThe solvent was removed in vacuum
  4. additionEthyl ether and water was added
  5. washThe organic phase was washed with water and brine
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated

Sources & evidence

ORD record
ord-68a91bf0489d44d0995b9b30830d34ef
Source dataset
uspto-grants-2014_12
Patent number
US08921359B2

Reaction notes

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