2,3-Dibromofuran → 5-(3-Bromofuran-2-yl)indan-1-one o-methyloxime
Reaction equation
Br[C:2]1[O:3][CH:4]=[CH:5][C:6]=1[Br:7].[CH3:8][O:9][N:10]=[C:11]1[C:19]2[C:14](=[CH:15][C:16](B(O)O)=[CH:17][CH:18]=2)[CH2:13][CH2:12]1>>[CH3:8][O:9][N:10]=[C:11]1[C:19]2[C:14](=[CH:15][C:16]([C:2]3[O:3][CH:4]=[CH:5][C:6]=3[Br:7])=[CH:17][CH:18]=2)[CH2:13][CH2:12]1Participants
3
Procedure
The title compound (1.6 g, 30%) was prepared from 2,3-dibromofuran and the product of Example 5 Step 6 using the method of Example 15 Step 1; 1H NMR (CDCl3) 7.88 (2H, m), 7.72 (1H, d, J 8.3 Hz), 7.42 (2H, d, J 3.1 Hz), 4.01 (3H, s), 3.17 (2H, m), 2.92 (2H, m).
Sources & evidence
- ORD record
- ord-db0c413ad62247989eb544813f9555b0
- Source dataset
- uspto-grants-2007_11
- Patent number
- US07297694B2
Reaction notes
Loading…