3,4-Dimethylpyridine → 1-(3-Chlorophenyl)-4-(3-methyl-4-pyridyl) butane
Reaction equation
[CH3:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[CH3:8].Br[CH2:10][CH2:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([Cl:19])[CH:14]=1>>[Cl:19][C:15]1[CH:14]=[C:13]([CH2:12][CH2:11][CH2:10][CH2:8][C:7]2[CH:6]=[CH:5][N:4]=[CH:3][C:2]=2[CH3:1])[CH:18]=[CH:17][CH:16]=1Participants
3
Procedure
1.0 g (9.35 mmol) of 3,4-dimethylpyridine and 2.18 g (9.35 mmol) of 1-bromo-3-(3-chlorophenyl)-propane were reacted in the same manner as in Example 26. The reaction product was purified to obtain 1.11 g of the desired compound (yield: 5.9%).
Workup
- customThe reaction product was purified
Sources & evidence
- ORD record
- ord-06c1c521d1b5456fa9c2c71a0f15490f
- Source dataset
- uspto-grants-1993_11
- Patent number
- US05262420
Reaction notes
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