Formaldehyde → HCID 20132564, compound
Reaction equation
[CH2:1]([N:8]([CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[OH:9])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:17]=O.[CH:19]([NH:22][CH:23]([CH3:25])[CH3:24])([CH3:21])[CH3:20]>>[CH2:10]([N:8]([CH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)[O:9][CH2:17][N:22]([CH:23]([CH3:25])[CH3:24])[CH:19]([CH3:21])[CH3:20])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1Participants
4
Procedure
The procedure of Example I is repeated using 21.33 g of dibenzylhydroxylamine, 9.73 g of aqueous formaldehyde (37%) solution and 10.12 g of diisopropylamine, to afford the title compound.
Sources & evidence
- ORD record
- ord-a05d2013b3244cf5b938c484b175fcad
- Source dataset
- uspto-grants-1988_07
- Patent number
- US04757102
Reaction notes
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