Hydrochloric Acid → HCID 23215434, compound
Reaction equation
[F:1][CH2:2][O:3][C:4]1[CH:9]=[CH:8][C:7](C(=O)C)=[CH:6][CH:5]=1.C1C=C(Cl)C=C(C(OO)=[O:21])C=1.[Li+].[OH-].Cl>ClCCl.C1COCC1.CO.O>[F:1][CH2:2][O:3][C:4]1[CH:9]=[CH:8][C:7]([OH:21])=[CH:6][CH:5]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of 1-(4-fluoromethoxy-phenyl)-ethanone (1.5 g; 8.9 mmol) in dichloromethane (30 mL) was added mCPBA (4.0 g; 17.8 mmol). The resulting mixture was stirred at room temperature for 4 h, then washed with saturated NaHCO3 (3×). The organic layer was dried over Na2SO4, concentrated under reduced pressure to give the crude material (3.77 g). The crude material (3.77 g) was dissolved in THF/MeOH/H2O (5/5/5 mL), then treated with LiOH (4.0 g; 108 mmol) at room temperature for 4 h. The reaction mixture was acidified with 2N HCl solution to pH 5. The mixture was extracted with EtOAc (3×). The organic phases were combined, dried over Na2SO4 and concentrated under reduced pressure to afford the title compound (1.3 g). This compound was used directly without further purification.
Workup
- washwashed with saturated NaHCO3 (3×)
- dry with materialThe organic layer was dried over Na2SO4
- concentrationconcentrated under reduced pressure
- customto give the crude material (3.77 g)
- extractionThe mixture was extracted with EtOAc (3×)
- dry with materialdried over Na2SO4
- concentrationconcentrated under reduced pressure
Sources & evidence
- ORD record
- ord-2ef2da2a620f4f1e894bff39e19fa4c5
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08685990B2
Reaction notes
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