Butylamine → N-Butyl-3,5-di-tert-butyl-4-hydroxybenzamide
Reaction equation
[CH2:1]([NH2:5])[CH2:2][CH2:3][CH3:4].[C:6]([C:10]1[CH:11]=[C:12]([CH:16]=[C:17]([C:20]([CH3:23])([CH3:22])[CH3:21])[C:18]=1[OH:19])[C:13](Cl)=[O:14])([CH3:9])([CH3:8])[CH3:7]>>[CH2:1]([NH:5][C:13](=[O:14])[C:12]1[CH:16]=[C:17]([C:20]([CH3:21])([CH3:22])[CH3:23])[C:18]([OH:19])=[C:10]([C:6]([CH3:9])([CH3:8])[CH3:7])[CH:11]=1)[CH2:2][CH2:3][CH3:4]Participants
3
Procedure
In the manner of Example 1, n-butylamine was reacted with 3,5-di-t-butyl-4-hydroxybenzoyl chloride to produce N-n-butyl-3,5-di-t-butyl-4-hydroxybenzamide; melting point 181°-183°C. When tested by the procedure in Example 2, the sample containing this compound lasted 950 hours, about 3.2 times as long as the control.
Sources & evidence
- ORD record
- ord-5b5a2b9ae8df44879fdaae947fc01d23
- Source dataset
- uspto-grants-1976_08
- Patent number
- US03972927
Reaction notes
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