Ammonia → Benzophenone imine
Reaction equation
[C:1]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH3:15]>C(C1C=CC=CC=1)(C)(C)C>[C:1](=[NH:15])([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
91.1 g of benzophenone, 150 ml of tert-butylbenzene and 2 g of 200-mesh silica-alumina (Nikki Kagaku K.K., N-635) were fed to the same reactor as in Example 11. The reactor was heated, and ammonia gas was continuously fed to the reactor at a feed rate of 1.5 Nl/min, while keeping the contents at 170° C, and reaction was carried out under 8 atm. for one hour. The withdrawn gas was cooled and condensed tert-butylbenzene was refluxed into the reactor. After the completion of the reaction, benzophenoneimine was obtained in yield of 28%.
Workup
- temperatureThe reactor was heated
- customat 170° C
- customreaction
- temperatureThe withdrawn gas was cooled
- temperaturewas refluxed into the reactor
- customAfter the completion of the reaction
Sources & evidence
- ORD record
- ord-106a027b0fac451a8d705b33e7c7208e
- Source dataset
- uspto-grants-1978_04
- Patent number
- US04083869
Reaction notes
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