3-Hydroxyacetophenone → 3-[1-Hydroxy-1-(4-methylphenyl)ethyl]phenol
Reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([C:8](=[O:10])[CH3:9])[CH:5]=[CH:6][CH:7]=1.[C:11]1([CH3:19])[CH:16]=[CH:15][C:14]([Mg]Br)=[CH:13][CH:12]=1>O1CCCC1>[OH:10][C:8]([C:4]1[CH:3]=[C:2]([OH:1])[CH:7]=[CH:6][CH:5]=1)([C:14]1[CH:15]=[CH:16][C:11]([CH3:19])=[CH:12][CH:13]=1)[CH3:9]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
By using 3′-hydroxyacetophenone (200 mg) and a 1 M solution of p-tolylmagnesium bromide in tetrahydrofuran (4.4 ml) as starting materials, the title compound (346.8 mg) was obtained in the same manner as that of Reference Example 69.
Sources & evidence
- ORD record
- ord-bf5280332a1845118e9b2b188eaf364c
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08293715B2
Reaction notes
Loading…