Hydrochloric Acid → Methyl 2-fluoro-3-iodo-4-methylbenzoate

HRID 1688309Notes

Reaction equation

HRID 1688309 reaction equation
[F:1][C:2]1[C:10]([I:11])=[C:9]([CH3:12])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].Cl.[CH3:14]O>>[F:1][C:2]1[C:10]([I:11])=[C:9]([CH3:12])[CH:8]=[CH:7][C:3]=1[C:4]([O:6][CH3:14])=[O:5]

Participants

4

Reactant 3

HCID 313Hydrochloric AcidHCID 887MethanolHCID 593839002-Fluoro-3-iodo-4-methylbenzoic acid

Product 1

HCID 67211177Methyl 2-fluoro-3-iodo-4-methylbenzoate

Conditions

Temperature
80 °C

Procedure

To the solution of 2-fluoro-3-iodo-4-methylbenzoic acid (450 mg, 1.6 mmol, 1.0 eq) in methanol (5 ml), catalytic amount of conc.HCl (0.1 ml) was added. The resultant solution was heated to reflux at 80° C. for overnight. Methanol was evaporated. To this residue, water was added and the aqueous layer was extracted thrice with ethyl acetate. The combined ethyl acetate extracts were dried over sodium sulphate, filtered and evaporated to afford methyl 2-fluoro-3-iodo-4-methylbenzoate. Yield: 450 mg (95%). 1H NMR (400 MHz, DMSO): δ 2.49 (s, 3H), 3.85 (s, 3H), 7.30-7.32 (d, 1H, J=7.84 Hz), 7.76-7.80 (t, 1H, J=7.82 Hz). LCMS: (ES+) m/z=295 (M+H).

Workup

  1. customMethanol was evaporated
  2. additionTo this residue, water was added
  3. extractionthe aqueous layer was extracted thrice with ethyl acetate
  4. dry with materialThe combined ethyl acetate extracts were dried over sodium sulphate
  5. filtrationfiltered
  6. customevaporated

Sources & evidence

ORD record
ord-cce69618c7c342a38dda11d6133bf01f
Source dataset
uspto-grants-2012_04
Patent number
US08148382B2

Reaction notes

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