Hydrochloric Acid → 4-(Piperazin-1-yl)benzoic acid hydrochloride
Reaction equation
C[O:2][C:3](=[O:16])[C:4]1[CH:9]=[CH:8][C:7]([N:10]2[CH2:15][CH2:14][NH:13][CH2:12][CH2:11]2)=[CH:6][CH:5]=1.[ClH:17]>>[ClH:17].[N:10]1([C:7]2[CH:6]=[CH:5][C:4]([C:3]([OH:16])=[O:2])=[CH:9][CH:8]=2)[CH2:11][CH2:12][NH:13][CH2:14][CH2:15]1Participants
3
Conditions
- Temperature
- 2 °C
Procedure
4-piperazin-1-yl-benzoic acid methyl ester (17 mmol) is dissolved in 6N HCl (25 ml) and heated under reflux for 3 hours. The mixture is cooled in an ice bath to 0-4° C. and the solid material formed is filtered off, washed with acetone and dried (vacuum). A white powder with mp. >240° C. is obtained.
Workup
- temperatureheated
- temperatureunder reflux for 3 hours
- customthe solid material formed
- filtrationis filtered off
- washwashed with acetone
- customdried (vacuum)
- customA white powder with mp. >240° C. is obtained
Sources & evidence
- ORD record
- ord-3527e5e768e14be3a0d0fb426d462b76
- Source dataset
- uspto-grants-2003_11
- Patent number
- US06642239B2
Reaction notes
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