3-Hydroxybenzophenone → HCID 69518274, compound
Reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([C:8]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[O:9])[CH:5]=[CH:6][CH:7]=1.CC(C)([O-])C.[K+].Cl[CH2:23][O:24][CH2:25][CH2:26][Si:27]([CH3:30])([CH3:29])[CH3:28]>C1COCC1>[C:10]1([C:8]([C:4]2[CH:5]=[CH:6][CH:7]=[C:2]([O:1][CH2:23][O:24][CH2:25][CH2:26][Si:27]([CH3:30])([CH3:29])[CH3:28])[CH:3]=2)=[O:9])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of (3-hydroxyphenyl)(phenyl)methanone (30.0 g, 151 mmole) in anhydrous THF (300 mL) at 0° C. was slowly added a solution of potassium-t-butoxide (200 mL-1 M in THF, 0.200 mmole), followed by a slow addition of [2-(chloromethoxy)ethyl](trimethyl)silane (32.1 mL, 182 mmole). After stirring the mixture for 2 h, the solvent was removed in vacuo and the residue redissolved in a mixture of H2O (200 mL) and EtOAc (200 mL). The aqueous layer was further extracted with EtOAc (2×100 mL). The combined extracts were washed with H2O (200 mL), 0.1 N HCl (500 mL), brine (100 mL), dried over MgSO4, filtered and concentrated in vacuo to give an orange oil. The crude product was redissolved in hexanes and filtered through a silica-gel plug to give the product as an impure pale yellow oil which is carried on without further purification: ESHRMS m/z 329.1586 (M+H, C19H25O3Si, Calc'd 329.1567).
Workup
- customthe solvent was removed in vacuo
- dissolutionthe residue redissolved in a mixture of H2O (200 mL) and EtOAc (200 mL)
- extractionThe aqueous layer was further extracted with EtOAc (2×100 mL)
- washThe combined extracts were washed with H2O (200 mL), 0.1 N HCl (500 mL), brine (100 mL)
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated in vacuo
- customto give an orange oil
- filtrationfiltered through a silica-gel plug
Sources & evidence
- ORD record
- ord-6f75107c5c2f4057929a81de3703d2ec
- Source dataset
- uspto-grants-2007_08
- Patent number
- US07259266B2
Reaction notes
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