3-Methoxybenzaldehyde → T-BUTYLNITRONE,A-(3-METHOXYPHENYL)
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][CH:10]=1)[CH:6]=O.[C:11]([NH:15][OH:16])([CH3:14])([CH3:13])[CH3:12]>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:6]=[N+:15]([C:11]([CH3:14])([CH3:13])[CH3:12])[O-:16])[CH:8]=[CH:9][CH:10]=1Participants
3
Procedure
The title compound was prepared according to the procedure described in Example 11 using 3-methoxybenzaldehyde and N-tert-butylhydroxylamine. The title compound was isolated in 56.5% overall yield as a crystalline solid, m.p. 93.4° C.
Workup
- customThe title compound was prepared
Sources & evidence
- ORD record
- ord-1c94fb85cace4737ab153fc1c2f0fb79
- Source dataset
- uspto-grants-2002_08
- Patent number
- US06433008B1
Reaction notes
Loading…