HCID 58707375, compound → 3-Acetyl-2-chloropyridine
Reaction equation
[Cl:1][C:2]1[N:20]=[CH:19][CH:18]=[CH:17][C:3]=1[C:4]([CH:6](C(OCC)=O)C(OCC)=O)=[O:5]>CS(C)=O.O>[Cl:1][C:2]1[C:3]([C:4](=[O:5])[CH3:6])=[CH:17][CH:18]=[CH:19][N:20]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 130 °C
Procedure
A solution of diethyl 2-(2-chloronicotinoyl)malonate (267 mmol) in dimethylsulfoxide (100 ml) was added dropwise over 1.5 h to a 130° C. solution of water (10 mL) in dimethylsulfoxide (260 mL). The reaction mixture was maintained at 130° C. for an additional 2 h and was allowed to cool to rt. The reaction mixture was diluted with cold (0° C.) water (500 mL) and was extracted with ethyl acetate (3×200 mL). The combined organic layers were washed with brine (5×200 mL), dried (sodium sulfate), and concentrated. The residue was purified by chromatography (10/1 petroleum ether/ethyl acetate) to provide 1-(2-chloropyridin-3-yl)ethanone 52% yield as yellow oil.
Workup
- temperatureto cool to rt
- extractionwas extracted with ethyl acetate (3×200 mL)
- washThe combined organic layers were washed with brine (5×200 mL)
- dry with materialdried (sodium sulfate)
- concentrationconcentrated
- customThe residue was purified by chromatography (10/1 petroleum ether/ethyl acetate)
Sources & evidence
- ORD record
- ord-d068526909e5489d820c6d26270a0329
- Source dataset
- uspto-grants-2012_01
- Patent number
- US08106066B2
Reaction notes
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