(4-Chlorophenyl)acetic acid → Ethyl 4-(4-chlorophenyl)-3-oxobutanoate
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([OH:11])=O)=[CH:4][CH:3]=1.[CH3:12][C:13]1(C)[O:18]C(=O)[CH2:16][C:15](=O)[O:14]1>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][C:9](=[O:11])[CH2:12][C:13]([O:14][CH2:15][CH3:16])=[O:18])=[CH:6][CH:7]=1Participants
3
Procedure
The title compound was prepared in 43% yield from 2-(4-chlorophenyl)acetic acid and 2,2-dimethyl-1,3-dioxane-4,6-dione according to the procedure for the preparation of Example 162, part A.
Sources & evidence
- ORD record
- ord-36dec81ae7bd410bb190e8e85b29fc9e
- Source dataset
- uspto-grants-2015_08
- Patent number
- US09107916B2
Reaction notes
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