3-Fluoroacetophenone → Ethyl 3-(3-fluorophenyl)-3-oxopropanoate
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([C:8](=[O:10])[CH3:9])[CH:5]=[CH:6][CH:7]=1.[CH2:11]([O:13][C:14](=[O:30])CC(C1C=CC(C2CCCCC2)=CC=1)=O)[CH3:12]>>[CH2:11]([O:13][C:14](=[O:30])[CH2:9][C:8]([C:4]1[CH:5]=[CH:6][CH:7]=[C:2]([F:1])[CH:3]=1)=[O:10])[CH3:12]Participants
3
Procedure
This compound was prepared from m-fluoro acetophenone, in a manner analogous to the preparation of 3-(4cyclohexylphenyl)-3-oxo-propionic acid ethyl ester (Method A), except that the product was purified by vacuum distillation (bp 114-117° C. at 0.8-0.9 mmHg) in 91% yield.
Workup
- distillationwas purified by vacuum distillation (bp 114-117° C. at 0.8-0.9 mmHg) in 91% yield
Sources & evidence
- ORD record
- ord-6143098e5d3f484ab2aebded6892def1
- Source dataset
- uspto-grants-2004_11
- Patent number
- US06815447B2
Reaction notes
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