2-Hydroxy-5-methoxybenzaldehyde → HCID 178492605, compound
Reaction equation
[OH:1][C:2]1[CH:9]=[CH:8][C:7]([O:10][CH3:11])=[CH:6][C:3]=1[CH:4]=O.[C:12]([NH:16][OH:17])([CH3:15])([CH3:14])[CH3:13]>>[OH:1][C:2]1[CH:9]=[CH:8][C:7]([O:10][CH3:11])=[CH:6][C:3]=1[CH:4]=[N+:16]([C:12]([CH3:15])([CH3:14])[CH3:13])[O-:17]Participants
3
Procedure
The title compound was prepared according to the procedure described in Example 1 using 2-hydroxy-5-methoxybenzaldehyde and N-tert-butylhydroxylamine. The title compound was isolated in 68.1 % yield as a crystalline solid, m.p. 70.4-71.6° C. (Rf=0.23 on a silica gel plate using 3:7 EtOAc/hexanes as an eluant).
Workup
- customThe title compound was prepared
Sources & evidence
- ORD record
- ord-4a6cd4e28cc14f5a8ac5318cc3afab63
- Source dataset
- uspto-grants-2001_03
- Patent number
- US06197826B1
Reaction notes
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