Methanol → (4-Iodo-2-(trifluoromethyl)phenyl)methanol

HRID 1946393Notes

Reaction equation

HRID 1946393 reaction equation
[I:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](O)=[O:7])=[C:4]([C:11]([F:14])([F:13])[F:12])[CH:3]=1.CO>C1COCC1>[I:1][C:2]1[CH:10]=[CH:9][C:5]([CH2:6][OH:7])=[C:4]([C:11]([F:12])([F:13])[F:14])[CH:3]=1

Participants

4

Conditions

Temperature
80 °C

Procedure

To a solution of 4-iodo-2-(trifluoromethyl)benzoic acid (for a preparation see Intermediate 31)(16.7 g, 52.8 mmol) in THF (150 ml) at ambient temperature under nitrogen was added 1.0 M borane-tetrahydrofuran complex (100 ml, 100 mmol, Aldrich) dropwise. The solution was heated to 80° C. for 1.5 h. To the solution at ambient temperature was added methanol (75 ml) and then heated to 80° C. for 1 h. The solvent was removed in vacuo to leave a mobile oil. The residue was partitioned between ethyl acetate (200 ml) and 2 N aqueous HCl (100 ml). The phases were separated and the organic phase washed with 2 N aqueous sodium hydroxide (100 ml), brine (50 ml), then dried (MgSO4), filtered and the solvent removed in vacuo to give [4-iodo-2-(trifluoromethyl)phenyl]methanol as a pale brown solid (14.8 g).

Workup

  1. customat ambient temperature
  2. additionwas added 1.0 M borane-tetrahydrofuran complex (100 ml, 100 mmol, Aldrich) dropwise
  3. temperatureheated to 80° C. for 1 h
  4. customThe solvent was removed in vacuo
  5. customto leave a mobile oil
  6. customThe residue was partitioned between ethyl acetate (200 ml) and 2 N aqueous HCl (100 ml)
  7. customThe phases were separated
  8. washthe organic phase washed with 2 N aqueous sodium hydroxide (100 ml), brine (50 ml)
  9. dry with materialdried (MgSO4)
  10. filtrationfiltered
  11. customthe solvent removed in vacuo

Sources & evidence

ORD record
ord-5b67c105aae14239811ad355b86de5e8
Source dataset
uspto-grants-2013_03
Patent number
US08399436B2

Reaction notes

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