Epichlorohydrin → HCID 54551003, compound
Reaction equation
[OH:1][C:2]1[CH:15]=[C:14]([OH:16])[CH:13]=[CH:12][C:3]=1[C:4]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)=[O:5].[CH2:17]([CH:19]1[O:21][CH2:20]1)Cl.[OH:22][CH:23]1[CH2:28][C:27]([CH3:30])([CH3:29])[N:26]([O:31][CH3:32])[C:25]([CH3:34])([CH3:33])[CH2:24]1>>[OH:1][C:2]1[CH:15]=[C:14]([O:16][CH2:17][CH:19]([OH:21])[CH2:20][O:22][CH:23]2[CH2:28][C:27]([CH3:29])([CH3:30])[N:26]([O:31][CH3:32])[C:25]([CH3:34])([CH3:33])[CH2:24]2)[CH:13]=[CH:12][C:3]=1[C:4]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)=[O:5]Participants
4
Procedure
The title compound is prepared by reaction of 2,4-dihydroxybenzophenone with epichlorohydrin followed by reaction with 4-hydroxy-1-methoxy-2,2,6,6-tetramethylpiperidine.
Sources & evidence
- ORD record
- ord-42cce49593f74ddbbcd0bef7b7f74489
- Source dataset
- uspto-grants-1991_06
- Patent number
- US05021478
Reaction notes
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