Benzyl Alcohol → 3,5-Dimethylbenzonitrile
Reaction equation
[C-]#N.[Na+].C[NH:5][CH2:6][CH2:7]NC.BrC1[CH:16]=[C:15]([CH3:17])[CH:14]=[C:13]([CH3:18])[CH:12]=1.C(O)C1C=CC=CC=1.CCCCCCCCCCCC.[OH-].[NH4+]>[Cu]I.O.C(OCC)(=O)C.C1(C)C=CC=CC=1>[CH3:18][C:13]1[CH:12]=[C:7]([CH:16]=[C:15]([CH3:17])[CH:14]=1)[C:6]#[N:5]Participants
Reactant 6
Product 1
Reagents, catalysts & solvents 4
Conditions
- Temperature
- 110 °C
Procedure
An oven dried screw cap test tube was charged with NaCN (140 mg, 2.857 mmol) dried KI (79 mg, 0.476 mmol, 20 mol %) and CuI (45 mg, 0.236 mmol, 10 mol %), evacuated and backfilled with argon three times. Anhydrous toluene (1550 μl), N,N′-dimethylethylenediamine (255 μl, 2.395 mmol), 1-Bromo-3,5-dimethyl-benzene (255 μl, 1.877 mmol), and benzyl alcohol (155 μl, 1.498 mmol) were added under argon. The tube was sealed and the reaction mixture was stirred magnetically at 110° C. for 12 h. The resulting yellow color suspension was cooled to room temperature, 2 mL of ethyl acetate, 250 μl of n-dodecane as internal standard, 1 mL of ammonium hydroxide 30% and 1 mL of water were added. The mixture was stirred at 25° C. for 10 min then the organic layer was washed with 1 mL of water and dried over MgSO4. The GC analysis showed a conversion of 91% with a yield of the title product, calculated vs internal standard, of 88%.
Workup
- customAn oven dried screw
- customcap test tube
- customevacuated
- customThe tube was sealed
- temperatureThe resulting yellow color suspension was cooled to room temperature
- stirringThe mixture was stirred at 25° C. for 10 min
- washthe organic layer was washed with 1 mL of water
- dry with materialdried over MgSO4
Sources & evidence
- ORD record
- ord-1563234a543b4cae92a7d5280e342688
- Source dataset
- uspto-grants-2005_05
- Patent number
- US06888032B2
Reaction notes
Loading…