HCID 15634761, compound → HCID 14835357, compound
Reaction equation
[CH2:1]([C:3]1[C:4]([NH2:17])=[C:5]([CH:14]=[CH:15][CH:16]=1)[C:6]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)=[O:7])[CH3:2]>C(O)(=O)C.OO>[CH2:1]([C:3]1[C:4]2[C:5](=[C:6]([C:8]3[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=3)[O:7][N:17]=2)[CH:14]=[CH:15][CH:16]=1)[CH3:2]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 7.5 g (0.033 mole) of 3-ethyl-2-aminobenzophenone in 150 ml of acetic acid and 40 ml of 30% hydrogen peroxide was let stand at ambient temperature for 72 hr. The solution was poured into ice water and a solid gradually crystallized. The solid was collected by filtration, washed with water and dried. The solid was then slurried with 20 ml of carbon tetrachloride and the mixture was filtered.
Workup
- customa solid gradually crystallized
- filtrationThe solid was collected by filtration
- washwashed with water
- customdried
- filtrationthe mixture was filtered
Sources & evidence
- ORD record
- ord-c0141e6713d94e4f99b92099a6bad3a7
- Source dataset
- uspto-grants-1990_02
- Patent number
- US04898874
Reaction notes
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