Hydrogen Bromide → HCID 45279909, compound
Reaction equation
[NH:1]([C:8]1[CH:25]=[CH:24][C:11]2[C:12](=[O:23])[C:13]3[CH:20]=[C:19]([O:21]C)[CH:18]=[CH:17][C:14]=3[CH2:15][CH2:16][C:10]=2[CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Br>C(O)(=O)C>[NH:1]([C:8]1[CH:25]=[CH:24][C:11]2[C:12](=[O:23])[C:13]3[CH:20]=[C:19]([OH:21])[CH:18]=[CH:17][C:14]=3[CH2:15][CH2:16][C:10]=2[CH:9]=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
0.2 g (0.61 mmol) of 2-anilino-7-methoxy-10,11-dihydrodibenzo[a,d]-cyclohepten-5-one is dissolved in 2 ml of glacial acetic acid, 2 ml of HBr (45%) are added and the mixture is refluxed for 6 h. The solution is hydrolyzed with 200 g of ice and the precipitate is filtered off. The product is obtained in the form of a white powder. C21H17NO2 (Mr=315.380)
Workup
- temperaturethe mixture is refluxed for 6 h
- filtrationthe precipitate is filtered off
- customThe product is obtained in the form of a white powder
Sources & evidence
- ORD record
- ord-c3d9d332f247473c834050612ea5af19
- Source dataset
- uspto-grants-2014_01
- Patent number
- US08633312B2
Reaction notes
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