4-Ethylpyridine → 1-(4-Bromophenyl)-3-(4-pyridyl)-butane
Reaction equation
[CH2:1]([C:3]1[CH:8]=[CH:7][N:6]=[CH:5][CH:4]=1)[CH3:2].[Br:9][C:10]1[CH:18]=[CH:17][C:13]([CH2:14][CH2:15]Br)=[CH:12][CH:11]=1>>[Br:9][C:10]1[CH:18]=[CH:17][C:13]([CH2:14][CH2:15][CH:1]([C:3]2[CH:8]=[CH:7][N:6]=[CH:5][CH:4]=2)[CH3:2])=[CH:12][CH:11]=1Participants
3
Procedure
1.0 g (9.35 mmol) of 4-ethylpyridine and 2.47 g (9.35 mmol) of 4-bromophenethyl bromide were reacted in the same manner as in Example 1. The reaction product was purified to obtain 1.10 g of the desired compound (yield: 40.7%).
Workup
- customThe reaction product was purified
Sources & evidence
- ORD record
- ord-b725b36d5ca04774ad2798ca293e30fc
- Source dataset
- uspto-grants-1993_11
- Patent number
- US05262420
Reaction notes
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