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Chemical Structure| 57554-82-2 Chemical Structure| 57554-82-2

Structure of 57554-82-2

Chemical Structure| 57554-82-2

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Product Details of [ 57554-82-2 ]

CAS No. :57554-82-2
Formula : C10H12ClNO2
M.W : 213.66
SMILES Code : CC(C1=CC=C(Cl)N=C1)C(OCC)=O

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Application In Synthesis of [ 57554-82-2 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 57554-82-2 ]

[ 57554-82-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 197376-47-9 ]
  • [ 74-88-4 ]
  • [ 57554-82-2 ]
YieldReaction ConditionsOperation in experiment
67% With sodium hydride; In N,N-dimethyl-formamide; at 0℃; for 1h; To a solution of <strong>[197376-47-9]ethyl 2-(6-chloropyridin-3-yl)acetate</strong> (1.1 g, 5.51 mmol) in dimethylformamide was added slowly sodium hydride (242 mg, 6.06 mmol) at 0 C, followed by iodomethane (821 mg, 5.79 mmol). The mixture was stirred at same degree for 1 hour, and then quenched with water. The resulting mixture was diluted with ethyl acetate and washed with water. The organic layer was dried over MgS04 and concentrated under reduced pressure to afford crude which was purified by column chromatography to afford ethyl 2-(6-chloropyridin-3-yl)propanoate (790 mg, 67 %).
67% With sodium hydride; In N,N-dimethyl-formamide; at 0℃; for 1h; To a solution of <strong>[197376-47-9]ethyl 2-(6-chloropyridin-3-yl)acetate</strong> (1.1 g, 5.51 mmol) in dimethylformamide was added slowly sodium hydride (242 mg, 6.06 mmol) at 0 C, followed by iodomethane (821 mg, 5.79 mmol). The mixture was stirred at same degree for 1 hour, and then quenched with water. The resulting mixture was diluted with ethyl acetate and washed with water. The organic layer was dried over magnesium sulphate and concentrated under reduced pressure to afford crude which was purified by column chromatography to afford ethyl 2-(6-chloropyridin-3-yl)propanoate (790 mg, 67 %).
67% With sodium hydride; In N,N-dimethyl-formamide; at 0℃; for 1h; Step 2: To a solution of <strong>[197376-47-9]ethyl 2-(6-chloropyridin-3-yl)acetate</strong> (1.1 g, 5.51 mmol) in dimethylformamide was added slowly sodium hydride (242 mg, 6.06 mmol) at 0 C., followed by iodomethane (821 mg, 5.79 mmol). The mixture was stirred at same degree for 1 hour, and then quenched with water. The resulting mixture was diluted with ethyl acetate and washed with water. The organic layer was dried over MgSO4 and concentrated under reduced pressure to afford crude which was purified by column chromatography to afford ethyl 2-(6-chloropyridin-3-yl)propanoate (790 mg, 67%).
67% With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 0℃; for 1h; Step 2 To a solution of <strong>[197376-47-9]ethyl 2-(6-chloropyridin-3-yl)acetate</strong> (1.1 g, 5.51 mmol) in dimethylformamide was added slowly sodium hydride (242 mg, 6.06 mmol) at 0 C., followed by iodomethane (821 mg, 5.79 mmol). The mixture was stirred at same degree for 1 hour, and then quenched with water. The resulting mixture was diluted with ethyl acetate and washed with water. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure to afford crude which was purified by column chromatography to afford ethyl 2-(6-chloropyridin-3-yl)propanoate (790 mg, 67%).
A solution of lithium bis(trimethylsilyl)amide in THF (1 M, 14 mL, 14.0 mmol) was added to a solution of <strong>[197376-47-9]ethyl 2-(6-chloropyridin-3-yl)acetate</strong> (2.5 g, 12.5 mmol) in THF at -78 C under nitrogen. After stirred at -78 C for 2 h, methyl iodide (1.94 g, 13.7 mmol) was added. The mixture was stirred at 20 C for another 8 h. Worked up, concentrated and purified with silica gelcolumn chromatography, eluting with 0%-40% EA/PE, to give the title compound (1.5 g, 83% purity in LCMS, yield 46%) as yellow oil. MS (ES+) C10H12C1N02 requires: 213, 215, found:214, 216 [M+H].

 

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