Hydrochloric Acid → 4-Aminobenzophenone
Reaction equation
[C:1]([C:9]1[CH:18]=[CH:17][C:12]([NH:13]C(=O)C)=[CH:11][CH:10]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.[OH-].[Na+]>>[NH2:13][C:12]1[CH:11]=[CH:10][C:9]([C:1]([C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[O:8])=[CH:18][CH:17]=1Participants
4
Procedure
p-Benzoylacetanilide (2.8 g.) and 100 ml. of 1N hydrochloric acid are refluxed for six hours. After cooling, the solution is made alkaline by the addition of 2N sodium hydroxide solution and extracted with ether to give 4-aminobenzophenone, which is recrystallized from methanol.
Workup
- temperatureAfter cooling
- extractionextracted with ether
Sources & evidence
- ORD record
- ord-a72f84d7ffd64c59ba1cab791580eabc
- Source dataset
- uspto-grants-1976_04
- Patent number
- US03949084
Reaction notes
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