4-Chloro-3-methylphenol → (S)-Methyl 2-(4-chloro-3-methylphenoxy)-3-methylbutanoate
Reaction equation
[OH:1][C@H:2]([CH:7]([CH3:9])[CH3:8])[C:3]([O:5][CH3:6])=[O:4].[Cl:10][C:11]1[CH:16]=[CH:15][C:14](O)=[CH:13][C:12]=1[CH3:18]>>[Cl:10][C:11]1[CH:16]=[CH:15][C:14]([O:1][C@@H:2]([CH:7]([CH3:9])[CH3:8])[C:3]([O:5][CH3:6])=[O:4])=[CH:13][C:12]=1[CH3:18]Participants
3
Procedure
The title compound was prepared following the same protocol as described in Step 1, Example 42, using the (R)-methyl 2-hydroxy-3-methylbutanoate instead of the (S)-methyl 2-hydroxypropanoate and the 4-chloro-3-methylphenol instead of the m-cresol.
Sources & evidence
- ORD record
- ord-aa1a7a5592744500bec2eefb733373ea
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09051265B2
Reaction notes
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