HCID 17989133, compound → HCID 17989219, compound
Reaction equation
[CH2:1]([O:3][C:4](=[O:20])[CH:5]([OH:19])[CH2:6][C:7]([C:10]1[CH:15]=[CH:14][C:13]([F:16])=[C:12]([O:17][CH3:18])[CH:11]=1)([CH3:9])[CH3:8])[CH3:2]>ClCCl>[CH2:1]([O:3][C:4](=[O:20])[C:5](=[O:19])[CH2:6][C:7]([C:10]1[CH:15]=[CH:14][C:13]([F:16])=[C:12]([O:17][CH3:18])[CH:11]=1)([CH3:9])[CH3:8])[CH3:2]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
2.78 g (9.78 mmol) of ethyl-4-(4-fluoro-3-methoxyphenyl)-2-hydroxy-4-methylpentanoate is oxidized as in Example 273 with SO3/Py in dichloromethane to the corresponding α ketoester. After chromatography on a Flashmaster, 2.48 g (89.9%) of the desired compound is obtained.
Sources & evidence
- ORD record
- ord-72a1d6244f7e429d8bcdcfaa3eaa2cd1
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07662821B2
Reaction notes
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