P-Anisidine → 3-(4-Methoxyanilino)-3-oxopropanoic acid
Reaction equation
[CH3:1][O:2][C:3]1[CH:9]=[CH:8][C:6]([NH2:7])=[CH:5][CH:4]=1.COC1C=CC=CC=1N[C:19](=[O:24])[CH2:20][C:21]([OH:23])=[O:22]>>[CH3:1][O:2][C:3]1[CH:9]=[CH:8][C:6]([NH:7][C:19](=[O:24])[CH2:20][C:21]([OH:23])=[O:22])=[CH:5][CH:4]=1Participants
3
Procedure
Starting from 4-methoxyaniline and following the procedure described above for the synthesis of compound 27 (example 8, scheme 8), title compound 157 was obtained in 56% yield. MS (m/z): 210.0 (M+H).
Sources & evidence
- ORD record
- ord-b61d08c965fe4291a514d48b58a98a2e
- Source dataset
- uspto-grants-2012_12
- Patent number
- US08329726B2
Reaction notes
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