Water → HCID 86748187, compound
Reaction equation
[N:1]1([C:15]2[CH:22]=[CH:21][C:18]([CH:19]=[O:20])=[CH:17][CH:16]=2)[CH2:6][CH2:5][N:4]([C:7]2[CH:14]=[CH:13][C:10]([CH:11]=[O:12])=[CH:9][CH:8]=2)[CH2:3][CH2:2]1.CC(C)=[O:25].OS(O)(=O)=O.O=[Cr](=O)=O.[OH2:36]>CC(C)=O>[N:1]1([C:15]2[CH:16]=[CH:17][C:18]([C:19]([OH:25])=[O:20])=[CH:21][CH:22]=2)[CH2:2][CH2:3][N:4]([C:7]2[CH:8]=[CH:9][C:10]([C:11]([OH:12])=[O:36])=[CH:13][CH:14]=2)[CH2:5][CH2:6]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 2 g of bis-4,4'-(1,4-piperazinediyl)dibenzaidehyde in 100 ml of acetone is treated dropwise with 100 ml of Jones' reagent. The mixture is stirred at room temperature for 1 hour and then poured into 100 ml of water. The precipitate which thereby results is filtered off, washed portionwise with water and dried in a vacuum. The crude product is recrystallized from ethanol and yields pure bis-4,4'-(1,4-piperazinediyl)dibenzoic acid.
Workup
- customThe precipitate which thereby results
- filtrationis filtered off
- washwashed portionwise with water
- customdried in a vacuum
- customThe crude product is recrystallized from ethanol
Sources & evidence
- ORD record
- ord-b7c99e4e70314eb5859da9f91a2d1562
- Source dataset
- uspto-grants-1994_10
- Patent number
- US05356559
Reaction notes
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