1-(2-Bromoethyl)-4-methoxybenzene → 1-Methoxy-4-(pent-4-en-1-yl)benzene
Reaction equation
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:6]([CH2:7][CH2:8][Mg]Br)=[CH:5][CH:4]=1.CO[C:15]1[CH:23]=CC(CCBr)=C[CH:16]=1.[Mg]>>[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:6]([CH2:7][CH2:8][CH2:23][CH:15]=[CH2:16])=[CH:5][CH:4]=1Participants
4
Procedure
This compound was prepared as in Example 35a using 4-methoxyphenethyl magnesium bromide prepared from 4-methoxyphenethyl bromide and magnesium turnings. The crude oil isolated after work-up was distilled to give the title compound (b.p. 65° C., 0.3 mm.Hg), as a colourless oil.
Workup
- customThis compound was prepared as in Example 35a
- customThe crude oil isolated after work-up
- distillationwas distilled
Sources & evidence
- ORD record
- ord-de0affe0b6de48ebaf00fb82f29584ce
- Source dataset
- uspto-grants-1986_04
- Patent number
- US04579862
Reaction notes
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