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Methanol → Methyl 3-bromo-4-ethylbenzoate

HRID 1434575
Notes
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Reaction equation

HRID 1434575 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[CH2:11][CH3:12])[C:5]([OH:7])=[O:6].OS(O)(=O)=O.[CH3:18]O>>[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[CH2:11][CH3:12])[C:5]([O:7][CH3:18])=[O:6]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 73033683-Bromo-4-ethylbenzoic acid

Product 1

HCID 13877473Methyl 3-bromo-4-ethylbenzoate

Procedure

3-Bromo-4-ethyl-benzoic acid (D43) (19.40 g) was dissolved in MeOH (200 mL) and then treated with conc. H2SO4 (1 mL). The mixture was heated at reflux overnight, and then concentrated under reduced pressure. The residue was partitioned between EtOAc and saturated aqueous NaHCO3 solution, extracting again with EtOAc. The combined extracts were then washed with brine, dried (MgSO4). The solvent was evaporated in vacuo to afford the title compound (15.8 g). 1H NMR (CDCl3) δ 1.24 (3H, t), 2.79 (2H, q), 3.91 (3H, s), 7.29 (1H, d), 7.89 (1H, dd), 8.19 (1H, d).

Workup

  1. temperature
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
The mixture was heated
  • temperatureat reflux overnight
  • concentrationconcentrated under reduced pressure
  • customThe residue was partitioned between EtOAc and saturated aqueous NaHCO3 solution
  • extractionextracting again with EtOAc
  • washThe combined extracts were then washed with brine
  • dry with materialdried (MgSO4)
  • customThe solvent was evaporated in vacuo
  • Sources & evidence

    ORD record
    ord-3adc8d2dfc3c40c3a0c56e97f84ec88a
    Source dataset
    uspto-grants-2009_11
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US07615550B2

    Reaction notes

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