Sulfuric Acid → 4-(1-Piperazinyl)benzamide
Reaction equation
[N:1]1([C:7]2[CH:14]=[CH:13][C:10]([C:11]#[N:12])=[CH:9][CH:8]=2)[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.S(=O)(=O)(O)[OH:16]>>[N:1]1([C:7]2[CH:8]=[CH:9][C:10]([C:11]([NH2:12])=[O:16])=[CH:13][CH:14]=2)[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1Participants
3
Procedure
To 8.0 g (0.04 mole) of 4-(1-piperazinyl)benzonitrile was added, with stirring, 50.0 ml (0.87 mole) of 93% sulfuric acid over a 15 min period. The mixture was stirred overnight and the resulting suspended amide was collected by filtration, rinsed with water, and allowed to air dry. The solid was recrystallized from absolute ethanol to give 1.6 g (20%) of white solid, m.p. 240°-243° C.
Workup
- stirringThe mixture was stirred overnight
- filtrationwas collected by filtration
- washrinsed with water
- customto air dry
- customThe solid was recrystallized from absolute ethanol
Sources & evidence
- ORD record
- ord-ccf9be2700804b9f877989ef09d562cc
- Source dataset
- uspto-grants-1989_11
- Patent number
- US04882330
Reaction notes
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