4-Hydroxybiphenyl → 4-(2-Bromoethoxy)-1,1'-biphenyl
Reaction equation
[C:1]1([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:6]=[CH:5][C:4]([OH:7])=[CH:3][CH:2]=1.C(OC(=O)[C@@H](OC)CC1C=CC(O[CH2:27][CH2:28][Br:29])=CC=1)C>>[Br:29][CH2:28][CH2:27][O:7][C:4]1[CH:3]=[CH:2][C:1]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[CH:6][CH:5]=1Participants
3
Procedure
The title compound was prepared from biphenyl-4-ol via the same procedure used for the preparation of (2S)-3-[4-(2-bromo-ethoxy)-phenyl]-2-methoxy-propionic acid ethyl ester (Example 283, Step 2) to produce a white solid. MS (ES) for C14H13BrO [M−H]−: 279.1.
Workup
- customto produce a white solid
Sources & evidence
- ORD record
- ord-a706c20f1f90480e95f7856cb5caa9be
- Source dataset
- uspto-grants-2007_03
- Patent number
- US07192982B2
Reaction notes
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