N-tert-butylhydroxylamine → HCID 178449916, compound
Reaction equation
[F:1][C:2]1[C:3]([OH:10])=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=O.[C:11]([NH:15][OH:16])([CH3:14])([CH3:13])[CH3:12]>>[F:1][C:2]1[C:3]([OH:10])=[C:4]([CH:5]=[N+:15]([C:11]([CH3:14])([CH3:13])[CH3:12])[O-:16])[CH:7]=[CH:8][CH:9]=1Participants
3
Procedure
The title compound was prepared according to the procedure described in Example 1 using 3-fluoro-2-hydroxybenzaldehyde and N-tert-butylhydroxylamine. The title compound was isolated in 92.7% yield as a yellow crystalline solid, m.p. 70.3° C. (Rf=0.25 on a silica gel plate using 7:3 hexanes/EtOAc as an eluant).
Workup
- customThe title compound was prepared
Sources & evidence
- ORD record
- ord-b624a19ca4144cbdbb4f1f90907f9131
- Source dataset
- uspto-grants-2001_03
- Patent number
- US06197826B1
Reaction notes
Loading…