3-(3-Hydroxy-phenyl)-2-methoxy-propionic acid methyl ester → (S)-3-(4-hydroxy-phenyl)-2-propoxy-propionic acid ethyl ester
Reaction equation
[CH2:1]([O:3][C:4](=[O:25])[C@@H:5]([O:21][CH2:22][CH2:23][CH3:24])[CH2:6][C:7]1[CH:12]=[CH:11][C:10]([O:13]CC2C=CC=CC=2)=[CH:9][CH:8]=1)[CH3:2].COC(=O)C(OC)CC1C=CC=C(O)C=1>>[CH2:1]([O:3][C:4](=[O:25])[C@@H:5]([O:21][CH2:22][CH2:23][CH3:24])[CH2:6][C:7]1[CH:8]=[CH:9][C:10]([OH:13])=[CH:11][CH:12]=1)[CH3:2]Participants
3
Procedure
The title compound was prepared from (2S)-3-(4-be yloxy-phenyl)-2-propoxy-propionic acid ethyl ester (Example 377, Step 3) via the same procedure used for the preparation of 3-(3-hydroxy-phenyl)-2-methoxy-propionic acid methyl ester (Example 291, Step 4) to produce a yellow oil. MS (ES) for C14H20O4 [M+H]+: 253.1.
Workup
- customto produce a yellow oil
Sources & evidence
- ORD record
- ord-e148863d2691420882b2f1d27e95f561
- Source dataset
- uspto-grants-2007_03
- Patent number
- US07192982B2
Reaction notes
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