[3-(Hydroxymethyl)phenyl]boronic acid → HCID 11559325, compound
Reaction equation
C([O:3][C:4](=[O:21])[CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([CH2:12][O:13][C:14]2[CH:19]=[CH:18][C:17](I)=[CH:16][CH:15]=2)[CH:7]=1)C.[OH:22][CH2:23][C:24]1[CH:25]=[C:26](B(O)O)[CH:27]=[CH:28][CH:29]=1>>[OH:22][CH2:23][C:24]1[CH:29]=[C:28]([C:17]2[CH:16]=[CH:15][C:14]([O:13][CH2:12][C:8]3[CH:7]=[C:6]([CH2:5][C:4]([OH:3])=[O:21])[CH:11]=[CH:10][CH:9]=3)=[CH:19][CH:18]=2)[CH:27]=[CH:26][CH:25]=1Participants
3
Procedure
[3-(3′-Hydroxymethyl-biphenyl-4-yloxymethyl)-phenyl]-acetic acid was prepared using general procedure 5 from [3-(4-iodo-phenoxymethyl)-phenyl]-acetic acid ethyl ester (of intermediate 4) and 3-(hydroxymethyl)phenylboronic acid (available from Aldrich Chemical Company, Inc., Milwaukee, Wis.). Mass spectrum MH+=349.
Sources & evidence
- ORD record
- ord-5b8f7ba7f652453b85de8e0ed5c300a9
- Source dataset
- uspto-grants-2009_04
- Patent number
- US07524870B2
Reaction notes
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