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Chemical Structure| 36853-14-2 Chemical Structure| 36853-14-2

Structure of 36853-14-2

Chemical Structure| 36853-14-2

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Product Details of [ 36853-14-2 ]

CAS No. :36853-14-2
Formula : C10H13NO3
M.W : 195.22
SMILES Code : O=C(C(C(C)=C1)=C(C)NC1=O)OCC
MDL No. :MFCD00514034

Safety of [ 36853-14-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H317-H319
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 36853-14-2 ]

* 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 [ 36853-14-2 ]

[ 36853-14-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 36853-14-2 ]
  • [ 54453-94-0 ]
YieldReaction ConditionsOperation in experiment
89% With trichlorophosphate; at 110℃; for 4h; (a) Ethyl 6-chloro-2,4-dimethylnicotinate; POCl3 (2.5 ml, 27 mmol) was added to ethyl 2,4-dimethyl-6-oxo~l,6-dihydropyridine-3- carboxylate [Chem. Pharm. Bull. Japan 1980, 28, 2244] (1.33 g, 6.8 mmol) and the mixture was heated at 110 C for 4 hours. The reaction was cooled and poured into ice and the excess POCl3 was allowed to react. The mixture was then extracted with EtOAc (2 x 100 ml) and the organic phase was washed with water (50 ml) and brine (50 ml). The solution was dried (Mg5O4). concentrated in vacuo and purified through a short plug of silica (10% EtOAc in hexanes) to provide ethyl 6-chloro-2,4-dimethylnicotinate. Yield: 1.30 g (89%). 1H NMR (400 MHz, CDCl3): 6 1.40 (3H, t, J= 7.1 Hz), 2.33 (3H, s), 2.53 (3H, s), 4.42 (2H-, q, J= 7.1 Hz)/7.05 (1H, s). M5 m/z: 214'(M+1).
89% With trichlorophosphate; at 110℃; for 4h; (a) Ethyl 6-chloro-2,4-dimethylnicotinate; POCl3 (2.5 ml, 27 mmol) was added to ethyl 2,4-dimethyl-6-oxo~l,6-dihydropyridine-3- carboxylate [Chem. Pharm. Bull. Japan 1980, 28, 2244] (1.33 g, 6.8 mmol) and the mixture was heated at 110 C for 4 hours. The reaction was cooled and poured into ice and the excess POCl3 was allowed to react. The mixture was then extracted with EtOAc (2 x 100 ml) and the organic phase was washed with water (50 ml) and brine (50 ml). The solution was dried (Mg5O4). concentrated in vacuo and purified through a short plug of silica (10% EtOAc in hexanes) to provide ethyl 6-chloro-2,4-dimethylnicotinate. Yield: 1.30 g (89%). 1H NMR (400 MHz, CDCl3): 6 1.40 (3H, t, J= 7.1 Hz), 2.33 (3H, s), 2.53 (3H, s), 4.42 (2H-, q, J= 7.1 Hz)/7.05 (1H, s). M5 m/z: 214'(M+1).
 

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