Sodium Hydroxide → HCID 20200705, compound
Reaction equation
C[O:2][C:3]([C:5]1[CH:24]=[CH:23][C:8]([CH2:9][N:10]([CH2:12][C:13]2[CH:18]=[CH:17][C:16]([C:19]([O:21]C)=[O:20])=[CH:15][CH:14]=2)[OH:11])=[CH:7][CH:6]=1)=[O:4].[OH-].[Na+]>>[C:3]([C:5]1[CH:6]=[CH:7][C:8]([CH2:9][N:10]([CH2:12][C:13]2[CH:18]=[CH:17][C:16]([C:19]([OH:21])=[O:20])=[CH:15][CH:14]=2)[OH:11])=[CH:23][CH:24]=1)([OH:4])=[O:2]Participants
3
Procedure
When N,N-bis(p-methoxycarbonylbenzyl)hydroxylamine, prepared in Example 1, is dissolved in an organic solvent and saponified with an aqueous sodium hydroxide solution, th above-named free acid compound is obtained after acidification with a mineral acid.
Workup
- dissolutionis dissolved in an organic solvent
- customis obtained after acidification with a mineral acid
Sources & evidence
- ORD record
- ord-66efd3eb04f04a5b8a29bfe4d9595091
- Source dataset
- uspto-grants-1987_05
- Patent number
- US04668727
Reaction notes
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