4-Hydroxyphenylacetone → 4-[2-(2,2,6,6-Tetramethylpiperidin-1-yl)ethoxy]phenyl acetone
Reaction equation
[CH3:1][C:2]1([CH3:13])[CH2:7][CH2:6][CH2:5][C:4]([CH3:9])([CH3:8])[N:3]1[CH2:10][CH2:11]Cl.[OH:14][C:15]1[CH:20]=[CH:19][C:18]([CH2:21][C:22](=[O:24])[CH3:23])=[CH:17][CH:16]=1>>[CH3:1][C:2]1([CH3:13])[CH2:7][CH2:6][CH2:5][C:4]([CH3:9])([CH3:8])[N:3]1[CH2:10][CH2:11][O:14][C:15]1[CH:16]=[CH:17][C:18]([CH2:21][C:22](=[O:24])[CH3:23])=[CH:19][CH:20]=1Participants
3
Procedure
Prepared from 2-(2,2,6,6-tetramethylpiperidin-1-yl)ethyl chloride and 4-hydroxyphenylacetone in a similar manner to Example 2 (b).
Sources & evidence
- ORD record
- ord-16aab6fe81254c02a64290af268a16e6
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07956084B2
Reaction notes
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