3-iodo-7-fluoro-5H-dibenzo[a,d]cyclohepten-5-one → 3-iodo-5H-dibenzo[a,d]cyclohepten-5-one
Reaction equation
[I:1][C:2]1[CH:3]=[CH:4][C:5]2[CH:11]=[CH:10][C:9]3[CH:12]=[CH:13][C:14](F)=[CH:15][C:8]=3[C:7](=[O:17])[C:6]=2[CH:18]=1.IC1C=CC2C=CC3C=CC(C)=CC=3C(=O)C=2C=1>>[I:1][C:2]1[CH:3]=[CH:4][C:5]2[CH:11]=[CH:10][C:9]3[CH:12]=[CH:13][CH:14]=[CH:15][C:8]=3[C:7](=[O:17])[C:6]=2[CH:18]=1Participants
3
Procedure
Following the procedure of Step B but substituting for the 3-amino-5H-dibenzo[ a,d]cyclohepten-5-one used therein an equimolecular amount of 3-amino-7-fluoro-5H-dibenzo[a,d]cyclohepten-5-one and 3-amino-7-methyl-5H-dibenzo[a,d]cyclohepten-5-one, there are produced respectively, 3-iodo-7-fluoro-5H-dibenzo[a,d]cyclohepten-5-one and 3-iodo-7-methyl-5H-dibenzo[a,d]cyclohepten-5-one.
Sources & evidence
- ORD record
- ord-5e4ecf219407457a97ce7223e676ccbe
- Source dataset
- uspto-grants-1977_06
- Patent number
- US04031223
Reaction notes
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