Hydrochloric Acid → HCID 67452576, compound
Reaction equation
C[O:2][C:3]1[N:8]=[C:7]([C:9]([CH3:13])([CH3:12])[C:10]#[N:11])[CH:6]=[CH:5][CH:4]=1.Cl>O1CCOCC1>[CH3:13][C:9]([C:7]1[NH:8][C:3](=[O:2])[CH:4]=[CH:5][CH:6]=1)([CH3:12])[C:10]#[N:11]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 190 °C
Procedure
To a 20 dram microwave vial was added 2-(6-methoxypyridin-2-yl)-2-methylpropanenitrile (7 g, 40 mmol) and 4N HCl in dioxane (15 mL). The reaction was then sealed and heated in a microwave reactor at 190° C. for 30 min. This reaction was repeated six times using the procedure above. These reactions were combined and filtered. The resultant white solid was washed with 20% EtOAc/hexanes and then dried in vacuo to afford 2-methyl-2-(6-oxo-1,6-dihydropyridin-2-yl)propanenitrile (24.7 g, 77%) as a white solid.
Workup
- customThe reaction was then sealed
- filtrationfiltered
- washThe resultant white solid was washed with 20% EtOAc/hexanes
- customdried in vacuo
Sources & evidence
- ORD record
- ord-3125debbbe4f406389c7ffee01232353
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08962632B2
Reaction notes
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