Cyclohexylhydroxylamine → alpha-(3,4Ethylenedioxyphenyl)-N-cyclohexylnitrone
Reaction equation
[CH2:1]1[CH2:12][O:11][C:10]2[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][C:3]=2[O:2]1.[CH:13]1([NH:19][OH:20])[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1>>[CH2:1]1[CH2:12][O:11][C:10]2[CH:9]=[CH:8][C:5]([CH:6]=[N+:19]([CH:13]3[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]3)[O-:20])=[CH:4][C:3]=2[O:2]1Participants
3
Procedure
The title compound was prepared according to the procedure described in Example 11 using 3,4ethylenedioxybenzaldehyde and N-cyclohexylhydroxylamine. The title compound was isolated in 74.5% yield as a solid, m.p. 96.7° C.
Workup
- customThe title compound was prepared
Sources & evidence
- ORD record
- ord-43083891f30e4e6c905b594687e2a20b
- Source dataset
- uspto-grants-2000_04
- Patent number
- US06046232
Reaction notes
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