2-Bromo-3-(4-fluorophenyl)-1-oxo-1H-inden-6-yl acetate → 2-Bromo-3-(4-fluorophenyl)-6-hydroxy-1H-inden-1-one
Reaction equation
C([O:4][C:5]1[CH:13]=[C:12]2[C:8]([C:9]([C:16]3[CH:21]=[CH:20][C:19]([F:22])=[CH:18][CH:17]=3)=[C:10]([Br:15])[C:11]2=[O:14])=[CH:7][CH:6]=1)(=O)C.C(OC1C=C2C(C(C3C=CC=CC=3)=C(Br)C2=O)=CC=1)(=O)C>>[Br:15][C:10]1[C:11](=[O:14])[C:12]2[C:8]([C:9]=1[C:16]1[CH:17]=[CH:18][C:19]([F:22])=[CH:20][CH:21]=1)=[CH:7][CH:6]=[C:5]([OH:4])[CH:13]=2Participants
3
Procedure
The procedure of Step 5 of Example 1 was repeated except for using 2-bromo-3-(4-fluorophenyl)-1-oxo-1H-inden-6-yl acetate obtained in Step 4 as a starting material instead of 2-bromo-1-oxo-3-phenyl-1H-inden-6-yl acetate and being stirred for 7 h to obtain the title compound (45%).
Sources & evidence
- ORD record
- ord-b4c390c671144f43bdcebf9a6023864f
- Source dataset
- uspto-grants-2014_11
- Patent number
- US08877747B2
Reaction notes
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