4'-Hydroxyacetophenone → 1-[4-(3-Chloropropoxy)phenyl]ethanone
Reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:10])[CH3:9])=[CH:4][CH:3]=1.Br[CH2:12][CH2:13][CH2:14][Cl:15].C(=O)([O-])[O-].[K+].[K+]>>[Cl:15][CH2:14][CH2:13][CH2:12][O:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:10])[CH3:9])=[CH:4][CH:3]=1Participants
4
Procedure
1-(4-hydroxyphenyl)ethanone, 1-bromo-3-chloropropane and potassium carbonate were processed as described in Example 67B to provide the title compound which was used in the next step without further purification.
Sources & evidence
- ORD record
- ord-4d21e46e291143f6beb388c318a3dc5e
- Source dataset
- uspto-grants-2003_02
- Patent number
- US06515013B2
Reaction notes
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