Isopropyl iodide → HCID 11369056, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][C:4]([CH3:7])=[CH:3][CH:2]=1.[CH:8]([I:11])([CH3:10])[CH3:9]>C(#N)C>[I-:11].[CH:8]([N+:1]1[CH:6]=[CH:5][C:4]([CH3:7])=[CH:3][CH:2]=1)([CH3:10])[CH3:9]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a stirred solution of 4-picoline (2.5 g, 26.8 mmol) in acetonitrile (50 ml) was added isopropyl iodide (9.1 g, 53.6 mmol) drop wise, the resultant mixture was heated at 90° C. for 24 hours. After cooling the solvent was evaporated to give a red solid which on trituration with ethyl acetate yielded 1-isopropyl-4-methylpyridinium iodide (6.01 g, 85%) as a cream solid, 1H NMR D6-DMSO δ?1.6 (d, 6H, J=7), 2.6 (s, 3H), 4.95 (m, 1H), 8.0 (d, 2H J=6), 9.05 (d, 2H J=6).
Workup
- temperatureAfter cooling the solvent
- customwas evaporated
- customto give a red solid which on trituration with ethyl acetate
Sources & evidence
- ORD record
- ord-6a8ae74af19f4ca3b498c77c625cec86
- Source dataset
- uspto-grants-2009_11
- Patent number
- US07618966B2
Reaction notes
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