Acetonitrile → HCID 22491023, compound
Reaction equation
[F:1]/[C:2](=[C:5](/[C:7]1[CH:16]=[C:15]2[C:10]([C:11](C)([CH3:20])[CH2:12]C=[C:14]2[CH:17]([CH3:19])[CH3:18])=[CH:9][C:8]=1OCC1CC1)\[CH3:6])/[CH2:3][OH:4].C[N+]1([O-])[CH2:33][CH2:32][O:31][CH2:30][CH2:29]1.ClCCl.[C:38](#N)[CH3:39]>[Ru]([O-])(=O)(=O)=O.C([N+](CCC)(CCC)CCC)CC>[F:1]/[C:2](=[C:5](/[C:7]1[CH:16]=[C:15]2[C:10]([C:11]([CH3:12])([CH3:20])[CH2:29][C:30]([O:31][CH2:32][CH:33]3[CH2:39][CH2:38]3)=[C:14]2[CH:17]([CH3:19])[CH3:18])=[CH:9][CH:8]=1)\[CH3:6])/[CH:3]=[O:4]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
As described in General Procedure H-1, (2E)-2-fluoro-3-(4,4-dimethyl-6-(cyclopropyl)methoxy-1-isopropyl-3,4-dihydronaphthalen-7-yl)-2-butenol (Compound A-54, 0.025 g, 0.070 mmol), tetrapropylammonium perruthenate (0.012 g, 0.038 mmol) and 4-methylmorpholine N-oxide (0.022 g, 0.19 mmol) were reacted in acetonitrile (0.2 mL) and dichloromethane (1 mL) to produce the title compound as an oil.
Sources & evidence
- ORD record
- ord-2921d095c69e4777a2652864dc98c797
- Source dataset
- uspto-grants-2005_05
- Patent number
- US06887896B1
Reaction notes
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