Imidazole → HCID 22244044, compound

HRID 577832Notes

Reaction equation

HRID 577832 reaction equation
[C:1]([Si:5](Cl)([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)([CH3:4])([CH3:3])[CH3:2].[F:19][C:20]1[C:25]([F:26])=[C:24]([F:27])[CH:23]=[CH:22][C:21]=1[CH2:28][OH:29].N1C=CN=C1>C(Cl)Cl>[C:1]([Si:5]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)[O:29][CH2:28][C:21]1[CH:22]=[CH:23][C:24]([F:27])=[C:25]([F:26])[C:20]=1[F:19])([CH3:4])([CH3:3])[CH3:2]

Participants

5

Procedure

tert-Butylchlorodiphenylsilane (8.86 ml, 34 mmol) was added slowly via syringe to a solution of (2,3,4-trifluorophenyl)methanol (5.0 g, 31 mmol) and imidazole (2.53 g, 37.2 mmol) in CH2Cl2 (30 ml) cooled in an ice water bath. The mixture warmed to room temperature and stir overnight. Solvent was removed and the residue was partitioned between Et2O and water. The Et2O was separated and washed with brine, and the combined aqueous layers were twice more extracted with Et2O, which was washed with brine. Drying (MgSO4) and removal of solvent gave an oil that was chromatographed on silica gel (50% CH2Cl2 in hexanes followed by gradient elution to 100% CH2Cl2) to isolate an oil that slowly solidified to afford 11.9 g (96%) of a white solid.

Workup

  1. temperaturecooled in an ice water bath
  2. customSolvent was removed
  3. customthe residue was partitioned between Et2O and water
  4. customThe Et2O was separated
  5. washwashed with brine
  6. extractionthe combined aqueous layers were twice more extracted with Et2O, which
  7. washwas washed with brine
  8. customDrying
  9. custom(MgSO4) and removal of solvent
  10. customgave an oil that
  11. customwas chromatographed on silica gel (50% CH2Cl2 in hexanes followed by gradient elution to 100% CH2Cl2)
  12. customto isolate an oil that

Sources & evidence

ORD record
ord-08187e34184749d6bbef82eb2bf2637e
Source dataset
uspto-grants-2015_05
Patent number
US09040528B2

Reaction notes

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