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4-Iodo-3-methylbenzoic acid → (4-Iodo-3-methylphenyl)methanol

HRID 2261796
Notes
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Reaction equation

HRID 2261796 reaction equation
[I:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](O)=[O:7])=[CH:4][C:3]=1[CH3:11]>C1COCC1>[I:1][C:2]1[CH:10]=[CH:9][C:5]([CH2:6][OH:7])=[CH:4][C:3]=1[CH3:11]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 15173224-Iodo-3-methylbenzoic acid

Product 1

HCID 53843601(4-Iodo-3-methylphenyl)methanolYield 95%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Procedure

To a solution of 4-Iodo-3-methyl-benzoic acid (5.2 g, 20 mmol) in THF (30 mL) is added 2.0 M borane-dimethyl sulfide complex in THF (40.0 mL, 80 mmol) dropwise. The mixture is stirred overnight. The reaction mixture is quenched carefully at 0° C. with methanol (20 mL) and the mixture is evaporated to dryness under reduced pressure. The residue is partitioned between EtOAc (80 mL) and water (60 mL). The organic phase is washed with brine (60 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure to a residue. The residue is purified by flash chromatography (gradient EtOAc/Hexane) to afford the title compound as white solid (4.7 g, 95%). 1HNMR (CDCl3) (ppm): 2.4 (3H, s), 4.55 (2H, s), 6.8-7.75 (3H, m).

Workup

  1. customThe reaction mixture is quenched carefully at 0° C. with methanol (20 mL)
  2. customthe mixture is evaporated to dryness under reduced pressure
  3. customThe residue is partitioned between EtOAc (80 mL) and water (60 mL)
  4. washThe organic phase is washed with brine (60 mL)
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure to a residue
  8. customThe residue is purified by flash chromatography (gradient EtOAc/Hexane)

Sources & evidence

ORD record
ord-713ab97a6e7d44c9901643bfca98c9e4
Source dataset
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07846960B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes