N-tert-butylhydroxylamine → alpha-(2,4,6-Triethoxyphenyl)-N-tert-butylnitrone
Reaction equation
[CH2:1]([O:3][C:4]1[CH:11]=[C:10]([O:12][CH2:13][CH3:14])[CH:9]=[C:8]([O:15][CH2:16][CH3:17])[C:5]=1[CH:6]=O)[CH3:2].[C:18]([NH:22][OH:23])([CH3:21])([CH3:20])[CH3:19]>>[CH2:1]([O:3][C:4]1[CH:11]=[C:10]([O:12][CH2:13][CH3:14])[CH:9]=[C:8]([O:15][CH2:16][CH3:17])[C:5]=1[CH:6]=[N+:22]([C:18]([CH3:21])([CH3:20])[CH3:19])[O-:23])[CH3:2]Participants
3
Procedure
The title compound was prepared according to the procedure described in Example 11 using 2,4,6-triethoxybenzaldehyde and N-tert-butylhydroxylamine. The title compound was isolated in 92.3% yield as a solid, m.p. 109.1° C.
Workup
- customThe title compound was prepared
Sources & evidence
- ORD record
- ord-3fb14f1eac77423e9f95db08d8a07d54
- Source dataset
- uspto-grants-2000_04