N-tert-butylhydroxylamine → HCID 178449925, compound
Reaction equation
[OH:1][C:2]1[CH:9]=[CH:8][C:7]([O:10][C:11]([F:14])([F:13])[F:12])=[CH:6][C:3]=1[CH:4]=O.[C:15]([NH:19][OH:20])([CH3:18])([CH3:17])[CH3:16]>>[OH:1][C:2]1[CH:9]=[CH:8][C:7]([O:10][C:11]([F:14])([F:13])[F:12])=[CH:6][C:3]=1[CH:4]=[N+:19]([C:15]([CH3:18])([CH3:17])[CH3:16])[O-:20]Participants
3
Procedure
The title compound was prepared according to the procedure described in Example 1 using 2-hydroxy-5-trifluoromethoxybenzaldehyde and N-tert-butylhydroxylamine. The title compound was isolated in 81.8% yield as a yellow crystalline solid, m.p. 82.6° C. (Rf=0.40 on a silica gel plate using 7:3 hexanes/EtOAc as an eluant).
Workup
- customThe title compound was prepared
Sources & evidence
- ORD record
- ord-a79f332626924f2fa1e3b0a54fef58ad
- Source dataset
- uspto-grants-2001_03
- Patent number
- US06197826B1
Reaction notes
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