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Methanol → Methyl 2-fluoro-3-methylbenzoate

HRID 1866916
Notes
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Reaction equation

HRID 1866916 reaction equation
[F:1][C:2]1[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].S(=O)(=O)(O)O.[CH3:17]O>>[F:1][C:2]1[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([O:6][CH3:17])=[O:5]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 27373792-Fluoro-3-methylbenzoic acid

Product 1

HCID 22049929Methyl 2-fluoro-3-methylbenzoateYield 82%

Procedure

To a solution of 2-fluoro-3-methyl benzoic acid (3.57 g, 23 mmol) in MeOH (40 mL) was added concentrated sulfuric acid (2.3 mL), and the reaction mixture was heated at reflux for 12 h. The reaction mixture was cooled, the solvent was removed under reduced pressure, and the residue was dissolved in EtOAc. The organic solution was washed with a saturated solution of NaHCO3 and then brine, dried (Na2SO4), filtered and concentrated under reduced pressure to afford methyl 2 fluoro-3-methylbenzoate as a yellow oil (3.2 g, 82%): 1H NMR (300 MHz, CDCl3) δ 7.76-7.71 (m, 1H), 7.39-7.34 (m, 1H), 7.08 (t, J=8 Hz, 1H), 3.98 (s, 3H), 2.31 (d, J=3 Hz, 3H).

Workup

  1. temperaturethe reaction mixture was heated
  2. temperatureat reflux for 12 h
  3. temperatureThe reaction mixture was cooled
  4. customthe solvent was removed under reduced pressure
  5. dissolutionthe residue was dissolved in EtOAc
  6. washThe organic solution was washed with a saturated solution of NaHCO3
  7. dry with materialbrine, dried (Na2SO4)
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-2c0230da45874d0db1f9d669bf94f7b7
Source dataset
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07629363B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes