2-Acetylhydroquinone → HCID 14983031, compound
Reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][C:3]=1[C:9](=[O:11])[CH3:10].[CH3:12][O:13][C:14]1[CH:15]=[C:16]([CH:20]=[CH:21][CH:22]=1)[C:17](Cl)=O.Br[CH2:24][CH2:25][CH2:26][CH2:27][CH2:28]Cl.[OH:30][CH:31]1[CH2:36][CH2:35][NH:34][CH2:33][CH2:32]1>>[OH:30][CH:31]1[CH2:36][CH2:35][N:34]([CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][O:8][C:5]2[CH:6]=[CH:7][C:2]3[O:1][C:17]([C:16]4[CH:20]=[CH:21][CH:22]=[C:14]([O:13][CH3:12])[CH:15]=4)=[CH:10][C:9](=[O:11])[C:3]=3[CH:4]=2)[CH2:33][CH2:32]1Participants
5
Procedure
The compound was prepared by a method similar to Example 11 from 2',5'-dihydroxyacetophenone, 3-methoxybenzoyl chloride, 1-bromo-5-chloropentane, and 4-hydroxypiperidine: mp 115°-116° C.
Sources & evidence
- ORD record
- ord-3adf3c4d293346f9a956ad4e6824915c
- Source dataset
- uspto-grants-1994_01
- Patent number
- US05278174
Reaction notes
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