2,4-Dihydroxybenzophenone → HCID 69422522, compound
Reaction equation
[CH2:1]([O:3][C:4](=[O:20])[C@@H:5]([O:18][CH3:19])[CH2:6][C:7]1[CH:12]=[CH:11][C:10]([O:13][CH2:14][CH2:15][CH2:16]Br)=[CH:9][CH:8]=1)[CH3:2].[OH:21][C:22]1[CH:35]=[C:34]([OH:36])[CH:33]=[CH:32][C:23]=1[C:24]([C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)=[O:25]>>[CH2:1]([O:3][C:4](=[O:20])[CH:5]([O:18][CH3:19])[CH2:6][C:7]1[CH:12]=[CH:11][C:10]([O:13][CH2:14][CH2:15][CH2:16][O:36][C:34]2[CH:33]=[CH:32][C:23]([C:24](=[O:25])[C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=3)=[C:22]([OH:21])[CH:35]=2)=[CH:9][CH:8]=1)[CH3:2]Participants
3
Procedure
A mixture of (2S)-3-[4-(3-Bromo-propoxy)-phenyl]-2-methoxy-propionic acid ethyl ester from Step A and 2,4-dihydroxybenzophenone were allowed to react under the Standard Procedure I to get to title compound.
Workup
- customto react under the Standard Procedure I
Sources & evidence
- ORD record
- ord-f46c47db909242c099bb8197249133e7
- Source dataset
- uspto-grants-2007_03
- Patent number
- US07192982B2
Reaction notes
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