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Chemical Structure| 1248195-40-5 Chemical Structure| 1248195-40-5

Structure of 1248195-40-5

Chemical Structure| 1248195-40-5

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Product Details of [ 1248195-40-5 ]

CAS No. :1248195-40-5
Formula : C11H13NO3
M.W : 207.23
SMILES Code : O=C(OCC)CC(C1=NC=CC=C1C)=O
MDL No. :MFCD16087887

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Application In Synthesis of [ 1248195-40-5 ]

* 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 [ 1248195-40-5 ]

[ 1248195-40-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 85279-30-7 ]
  • [ 105-58-8 ]
  • [ 1248195-40-5 ]
YieldReaction ConditionsOperation in experiment
85% With sodium hydride; In mineral oil; at 90℃; for 4h; To a stirred solution of <strong>[85279-30-7]1-(3-methylpyridin-2-yl)ethanone</strong> (500 mg, 3.70 mmol, 1 eq) in diethyl carbonate (30 ml) was added NaH (60% in oil, 887.6 mg, 22.2 mmol, 6 eq) protionwise at 25 oC. The grey suspension was then stirred at 90 oC for 4 hours. Acetic acid (2.1 ml) in diethyl ether (21 ml) was added dropwise to quench the reaction. The resulting mixture was filtered through a pad of celite. The filtrate was concentrated and purified on silica gel (80 g) with a gradient of ethyl acetate in hexanes from 0 : 1 to 3 : 7 to give a dark brown oil (650 mg, 85%). 1H NMR (300 MHz, CDCl3): delta 8.52-8.46 (m, 1H), 7.63-7.59 (m, 1H), 7.35 (dd, J = 7.9, 4.5 Hz, 1H), 4.24-4.10 (m, 4H), 2.63 (s, 3H), 1.23 (t, J = 7.0 Hz, 3H); Calculated for C11H13NO3, 207.09; MS (ESI) (m/z) observed 208.2 (M + 1)+.
85% With sodium hydride; In mineral oil; at 25 - 90℃; for 4h; To a stirred solution of <strong>[85279-30-7]1-(3-methylpyridin-2-yl)ethanone</strong> (500 mg, 3.70 mmol, 1 eq) in diethyl carbonate (30 ml) was added NaH (60% in oil, 887.6 mg, 22.2 mmol, 6 eq) protionwise at 25 C. The grey suspension was then stirred at 90 C for 4 hours. Acetic acid (2.1 ml) in diethyl ether (21 ml) was added dropwise to quench the reaction. The resulting mixture was filtered through a pad of celite. The filtrate was concentrated and purified on silica gel (80 g) with a gradient of ethyl acetae in hexances from 0 : 1 to 3 : 7 to give a dark brown oil (650 mg, 85%). NMR (300 MHz, CDCh): delta 8.52-8.46 (m, 1H), 7.63-7.59 (m, 1H), 7.35 (dd, J = 7.9, 4.5 Hz, 1H), 4.24-4.10 (m, 4H), 2.63 (s, 3H), 1.23 (t, J = 7.0 Hz, 3H); Calculated for CI 1H13N03, 207.09; MS (ESI) (m/z) observed 208.2 (M + 1)+.
 

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