Acetic Acid → HCID 19827430, compound
Reaction equation
[N+:1]([C:4]1[C:5]([NH2:14])=[C:6]([OH:13])[CH:7]=[CH:8][C:9]=1CCBr)([O-:3])=[O:2].[CH3:15][NH:16][CH3:17].O.[C:19](O)(=O)[CH3:20]>>[N+:1]([C:4]1[C:5]([NH:14][CH2:19][CH3:20])=[C:6]([OH:13])[CH:7]=[CH:8][C:9]=1[N:16]([CH3:17])[CH3:15])([O-:3])=[O:2]Participants
5
Procedure
0.0766 mol (20 g) of 3-nitro-4-(β-bromoethyl)-aminophenol is heated for 20 minutes, at 60° C., in 60 ml of a 40% strength aqueous solution of dimethylamine. The reaction medium is poured into 300 ml of iced water and then neutralised with acetic acid. The expected product precipitates. It is filtered off, washed with water and recrystallised from ethanol. After drying in vacuo, it melts at 151° C.
Workup
- customThe expected product precipitates
- filtrationIt is filtered off
- washwashed with water
- customrecrystallised from ethanol
- customAfter drying in vacuo, it melts at 151° C.
Sources & evidence
- ORD record
- ord-ea0a4193d0a14e18a27f8ae10c37e822
- Source dataset
- uspto-grants-1991_06
- Patent number
- US05026401
Reaction notes
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