HCID 69116784, compound → HCID 58629987, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:13]([O:14]C)=[CH:12][CH:11]=[CH:10][C:9]=2[F:16])=[C:4]([CH3:17])[CH:3]=1>Br>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:13]([OH:14])=[CH:12][CH:11]=[CH:10][C:9]=2[F:16])=[C:4]([CH3:17])[CH:3]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
Treatment of 4-chloro-2′-fluoro-6′-methoxy-2-methylbiphenyl (2.7 g, 10.8 mmol) with hydrogen bromide (33% in acetic acid, 50 mL) according to the procedure described for Example 69, Step 2 provided 2.2 g (86%) of 4′-chloro-6-fluoro-2′-methylbiphenyl-2-ol as a colorless oil.
Sources & evidence
- ORD record
- ord-28d0f769045444dd8ff0dfd83806b619
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07365095B2
Reaction notes
Loading…