Butyryl chloride → HCID 136393675, compound
Reaction equation
[C:1]([C:5]1[CH:6]=[C:7]([CH:17]=[C:18]([C:21]([CH3:24])([CH3:23])[CH3:22])[C:19]=1[OH:20])[C:8](=[N:15][OH:16])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)([CH3:4])([CH3:3])[CH3:2].[C:25](Cl)(=[O:29])[CH2:26][CH2:27][CH3:28]>>[C:25]([O:16][N:15]=[C:8]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[C:7]1[CH:17]=[C:18]([C:21]([CH3:24])([CH3:23])[CH3:22])[C:19]([OH:20])=[C:5]([C:1]([CH3:4])([CH3:3])[CH3:2])[CH:6]=1)(=[O:29])[CH2:26][CH2:27][CH3:28]Participants
3
Procedure
3,5-di-t-butyl-4-hydroxybenzophenone oxime and butyryl chloride were treated in the same way as in Example 3 to give 3,5-di-t-butyl-4-hydroxybenzophenone O-butyryloxime.
Sources & evidence
- ORD record
- ord-e3fcb49c4e3743aa85f7c167b2ff1443
- Source dataset
- uspto-grants-1987_06
- Patent number
- US04673692
Reaction notes
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