Potassium Carbonate → 4-(2-Hydroxy-2-methyl-propoxy)benzonitrile

HRID 713079Notes

Reaction equation

HRID 713079 reaction equation
Cl[CH2:2][C:3]([CH3:6])([OH:5])[CH3:4].[OH:7][C:8]1[CH:15]=[CH:14][C:11]([C:12]#[N:13])=[CH:10][CH:9]=1.C([O-])([O-])=O.[K+].[K+]>O.C(O)C>[OH:5][C:3]([CH3:6])([CH3:4])[CH2:2][O:7][C:8]1[CH:15]=[CH:14][C:11]([C:12]#[N:13])=[CH:10][CH:9]=1

Participants

6

Conditions

Temperature
80 °C

Procedure

A mixture of 1-chloro-2-methyl-propan-2-ol (10 mL), 4-hydroxybenzonitrile (2 g, 16.8 mmol), K2CO3 (9.3 g, 67.3 mmol) in water (6 mL) and ethanol (60 mL) was heated at 80° C. for 16 hours. The reaction mixture was cooled and the solvent was concentrated in vacuo. The residue was diluted with ether (200 mL) and filtered and the filtrate was washed sequentially with water (50 mL) and brine solution (50 mL). The organics were separated and dried over MgSO4 and solvent was removed in vacuo to give a residue which was purified by silica gel column chromatography using (0-100%) EtOAc/DCM as eluent to give 4-(2-hydroxy-2-methyl-propoxy)benzonitrile (3.0 g, 94%) as a yellow solid. ESI-MS m/z calc. 191.1. found 192.3 (M+1)+; Retention time: 1.05 minutes (3 min run).

Workup

  1. temperatureThe reaction mixture was cooled
  2. concentrationthe solvent was concentrated in vacuo
  3. additionThe residue was diluted with ether (200 mL)
  4. filtrationfiltered
  5. washthe filtrate was washed sequentially with water (50 mL) and brine solution (50 mL)
  6. customThe organics were separated
  7. dry with materialdried over MgSO4 and solvent
  8. customwas removed in vacuo
  9. customto give a residue which
  10. customwas purified by silica gel column chromatography

Sources & evidence

ORD record
ord-c9d79cb0c8f6482cb2cc5c675351c431
Source dataset
uspto-grants-2015_11
Patent number
US09181273B2

Reaction notes

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