1,3-Dibromopropane → Methyl 3-[4-(3-bromopropoxy)-2-methoxyphenyl]heptanoate
Reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH2:14][CH2:15][CH2:16][CH3:17])[CH2:9][C:10]([O:12][CH3:13])=[O:11])=[C:4]([O:18][CH3:19])[CH:3]=1.[Br:20][CH2:21][CH2:22][CH2:23]Br>>[Br:20][CH2:21][CH2:22][CH2:23][O:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH2:14][CH2:15][CH2:16][CH3:17])[CH2:9][C:10]([O:12][CH3:13])=[O:11])=[C:4]([O:18][CH3:19])[CH:3]=1Participants
3
Procedure
Following a similar procedure to that described in Preparation 45A(i), but using methyl 3-(4-hydroxy-2-methoxyphenyl)heptanoate (prepared as described in Preparation 58A) and 1,3-dibromopropane, methyl 3-[4-(3-bromopropoxy)-2-methoxyphenyl]heptanoate was obtained as an oily substance.
Workup
- customthat described in Preparation 45A(i)
Sources & evidence
- ORD record
- ord-7a8a94b8a7684f6eadb04f1310ddd605
- Source dataset
- uspto-grants-2000_03
- Patent number
- US06040339
Reaction notes
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