Benzaldehyde, 2-ethoxy- → alpha-(Ethoxyphenyl)-N-cyclohexylnitrone
Reaction equation
[CH2:1]([O:3][C:4]1[CH:11]=[CH:10][CH:9]=[CH:8][C:5]=1[CH:6]=O)[CH3:2].[CH:12]1([NH:18][OH:19])[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]1>>[CH2:1]([O:3][C:4]1[CH:11]=[CH:10][CH:9]=[CH:8][C:5]=1[CH:6]=[N+:18]([CH:12]1[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]1)[O-:19])[CH3:2]Participants
3
Procedure
The title compound was prepared according to the procedure described in Example 11 using 2-ethoxybenzaldehyde and N-cyclohexylhydroxylamine. The title compound was isolated in 89% yield as a solid. m.p. 54.8° C.
Workup
- customThe title compound was prepared
Sources & evidence
- ORD record
- ord-633a1038e21d4375adfd3160cbce7d7a
- Source dataset
- uspto-grants-2002_08
- Patent number
- US06433008B1
Reaction notes
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