Thionyl Chloride → 6-Methoxy-1-Indanone
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][C:11]([OH:13])=O)=[CH:5][CH:4]=1.S(Cl)(Cl)=O.[Cl-].[Al+3].[Cl-].[Cl-]>C(Cl)Cl>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:6]([CH2:9][CH2:10][C:11]2=[O:13])=[CH:7][CH:8]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
To a solution of 3-(4-methoxyphenyl)propionic acid (50.34 g, 0,279 mol) in 500 mL of methylene chloride cooled to 0° C. was added slowly at 0° C. 30.5 mL (0.418 mol) of thionyl chloride, the mixture was stirred 10 h at room temperature and the solvent was removed in vacuo. The residue was dissolved in 1000 mL of methylene chloride, cooled to 0° C., and 40.92 g (0.306 mol) of aluminum chloride was added in small portions and the resulting mixture was stirred at room temperature for 1 h. The above mixture was poured onto ice, the resulting mixture was filtered through celite, and the aqueous layer was extracted with methylene chloride (2×200 mL). The combined organic layer was dried over sodium sulfate, concentrated in vacuo, and the residue was extracted with hexane to afford 40 g (88%) of 6-methoxy-1-indanone.
Workup
- additionwas added slowly at 0° C
- customthe solvent was removed in vacuo
- dissolutionThe residue was dissolved in 1000 mL of methylene chloride
- additionThe above mixture was poured onto ice
- filtrationthe resulting mixture was filtered through celite
- extractionthe aqueous layer was extracted with methylene chloride (2×200 mL)
- dry with materialThe combined organic layer was dried over sodium sulfate
- concentrationconcentrated in vacuo
- extractionthe residue was extracted with hexane
Sources & evidence
- ORD record
- ord-d19787a5655e4f4ca1c2bc4a2507cb7a
- Source dataset
- uspto-grants-1996_09
- Patent number
- US05554620
Reaction notes
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