2-Fluorophenyltributyltin → 3,4-Dihydro-7-fluoro-6-(2-fluorophenyl)-1(2H)-naphthalenone
Reaction equation
[F:1][C:2]1[CH:11]=[C:10]2[C:5]([CH2:6][CH2:7][CH2:8][C:9]2=[O:12])=[CH:4][C:3]=1OS(C(F)(F)F)(=O)=O.[F:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=1[Sn](CCCC)(CCCC)CCCC>>[F:1][C:2]1[CH:11]=[C:10]2[C:5]([CH2:6][CH2:7][CH2:8][C:9]2=[O:12])=[CH:4][C:3]=1[C:23]1[CH:24]=[CH:25][CH:26]=[CH:27][C:22]=1[F:21]Participants
3
Procedure
Using 1.50 g (4.80 mmol) of 3,4-dihydro-7-fluoro-6-trifluoromethylsulfonyloxy-1(2H)-naphthalenone and 2.22 g (5.78 mmol) of 2-fluorophenyltributyltin, the same reaction as described in Reference Example 1 was carried out to obtain 0.66 g of the above-mentioned compound (yield 53%).
Workup
- customthe same reaction
Sources & evidence
- ORD record
- ord-47c62c4d73124b5c971d0d5371738cdd
- Source dataset
- uspto-grants-1997_07
- Patent number
- US05646283
Reaction notes
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