HCID 21568772, compound → HCID 21568801, compound
Reaction equation
[CH2:1]([CH:3]([C:12]1[CH:13]=[C:14]([OH:19])[CH:15]=[C:16]([CH:18]=1)[OH:17])[CH:4]([CH2:10][CH3:11])[CH2:5][CH2:6][CH2:7][CH2:8][CH3:9])[CH3:2].[C:20]([CH:23]1[CH2:28][CH2:27][CH:26]([CH3:29])[CH2:25][C:24]1=O)(=O)[CH3:21]>>[CH2:1]([CH:3]([C:12]1[CH:18]=[C:16]([OH:17])[C:15]2[CH:20]([CH3:21])[C:23]3[CH2:28][CH2:27][CH:26]([CH3:29])[CH2:25][C:24]=3[O:19][C:14]=2[CH:13]=1)[CH:4]([CH2:10][CH3:11])[CH2:5][CH2:6][CH2:7][CH2:8][CH3:9])[CH3:2]Participants
3
Procedure
Condensation of 5-(1,2-diethylheptyl)resorcinol and 2-acetyl-5-methylcyclohexanone as described in the procedure of Example 1 gives the title compound.
Sources & evidence
- ORD record
- ord-bf21819f6b6a4eaf9d2f624725395f4b
- Source dataset
- uspto-grants-1976_01
- Patent number
- US03931232
Reaction notes
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