Methanol → Methyl 3-bromo-4-methylbenzoate

HRID 1052049Notes

Reaction equation

HRID 1052049 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[CH3:11])[C:5]([OH:7])=[O:6].S(=O)(=O)(O)O.[CH3:17]O>>[CH3:17][O:6][C:5](=[O:7])[C:4]1[CH:8]=[CH:9][C:10]([CH3:11])=[C:2]([Br:1])[CH:3]=1

Participants

4

Conditions

Temperature
60 °C

Procedure

A suspension of 3-bromo-4-methylbenzoic acid (2.0 g, 9.30 mmol) in methanol (20 ml) was treated with sulfuric acid (0.04 ml) and the reaction mixture was stirred at 60° C. for 42 hours. The reaction mixture was concentrated and the residue was taken up in ethyl acetate. The organic solution was washed with sat'd NaHCO3(aq.), dried (MgSO4), filtered, and concentrated to give the title compound as an orange oil which was suitable for use without further purification (2.25 g, quant.).

Workup

  1. concentrationThe reaction mixture was concentrated
  2. washThe organic solution was washed with sat'd NaHCO3(aq.)
  3. dry with materialdried (MgSO4)
  4. filtrationfiltered
  5. concentrationconcentrated

Sources & evidence

ORD record
ord-bea6c741009d43dcbedcecd1b5036dca
Source dataset
uspto-grants-2016_07
Patent number
US09388176B2

Reaction notes

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