α,4′-Dihydroxy[1,1′-biphenyl]-4-acetic acid → HCID 21556546, compound
Reaction equation
N[C:2]1[CH:3]=[C:4]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH:5]=[CH:6][C:7]=1[CH:8]([OH:14])[C:9]([O:11]CC)=[O:10].NC1C=CC(C2C=CC(C(O)C(OCC)=[O:36])=CC=2)=CC=1.OC1C=C(C2C=CC=CC=2)C=CC=1C(O)C(O)=O.OC1C=CC(C2C=CC(C(O)C(O)=O)=CC=2)=CC=1>>[OH:36][C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=1[C:4]1[CH:5]=[CH:6][C:7]([CH:8]([OH:14])[C:9]([OH:11])=[O:10])=[CH:2][CH:3]=1Participants
5
Procedure
When ethyl 3-amino-4-biphenylylglycolate or ethyl 4'-amino-4-biphenylylglycolate are used in the above procedure then the product prepared is 3-hydroxy-4-biphenylylglycolic acid or 4'-hydroxy-4-biphenylylglycolic acid.
Workup
- customthe product prepared
Sources & evidence
- ORD record
- ord-642b6d737e1d47418adcd73baa8e5635
- Source dataset
- uspto-grants-1976_03
- Patent number
- US03941821
Reaction notes
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