Octylamine → HCID 54477789, compound
Reaction equation
[CH2:1]([NH2:9])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[C:10]([C:14]1[CH:15]=[C:16]([CH:33]=[C:34]([C:37]([CH3:40])([CH3:39])[CH3:38])[C:35]=1[OH:36])[C:17]([O:19][C:20]1[C:28]([C:29]([CH3:32])([CH3:31])[CH3:30])=[CH:27][C:23]([C:24](Cl)=[O:25])=[CH:22][CH:21]=1)=[O:18])([CH3:13])([CH3:12])[CH3:11]>>[CH2:1]([NH:9][C:24](=[O:25])[C:23]1[CH:27]=[C:28]([C:29]([CH3:32])([CH3:31])[CH3:30])[C:20]([O:19][C:17](=[O:18])[C:16]2[CH:15]=[C:14]([C:10]([CH3:12])([CH3:11])[CH3:13])[C:35]([OH:36])=[C:34]([C:37]([CH3:40])([CH3:39])[CH3:38])[CH:33]=2)=[CH:21][CH:22]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]Participants
3
Procedure
Following the procedure of Example 8, n-octylamine is reacted with 4-(3,5-di-t-butyl-4-hydroxybenzoyloxy)-5-t-butylbenzoyl chloride to yield N-n-octyl-4-(3,5-di-t-butyl-4-hydroxybenzoyloxy)-5-t-butylbenzamide.
Sources & evidence
- ORD record
- ord-bc152d37873d460db46bef34b88f7b7c
- Source dataset
- uspto-grants-1976_09
- Patent number
- US03979360
Reaction notes
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