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Chemical Structure| 1214340-74-5 Chemical Structure| 1214340-74-5

Structure of 1214340-74-5

Chemical Structure| 1214340-74-5

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Product Details of [ 1214340-74-5 ]

CAS No. :1214340-74-5
Formula : C6H5Cl2NO
M.W : 178.02
SMILES Code : COC1=CC=C(Cl)N=C1Cl
MDL No. :MFCD13185542

Safety of [ 1214340-74-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H320-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 1214340-74-5 ]

* 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 [ 1214340-74-5 ]

[ 1214340-74-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 148493-34-9 ]
  • [ 1214340-74-5 ]
  • 2
  • [ 52764-11-1 ]
  • [ 74-88-4 ]
  • [ 1214340-74-5 ]
YieldReaction ConditionsOperation in experiment
96.0% With potassium carbonate; In N,N-dimethyl-formamide; at 80℃; for 2h; To a solution of <strong>[52764-11-1]2,6-dichloropyridin-3-ol</strong> (16.3 g, 0.1 mol) and K2C03 (41.4 g, 0.3 mol) in DMF (200 mL) were added Mel (21.3 g, 0.15 mol). The mixture was allowed to stir at 80 C for 2 hours. The mixture was then diluted with water (200 mL) and extracted with EtOAc (200 mL x 3). The organic layer was washed with brine (200 mL x 3), dried over Na2S04, filtered and the solvent was evaporated to provide 2,6-dichloro-3-methoxypyridine (17.0 g, yield: 96.0%). 1H-NMR (CDC13, 400 MHz) delta 7.12-7.18 (m, 2H), 3.86 (s, 3H).
96% With potassium carbonate; In N,N-dimethyl-formamide; at 80℃; for 2h; To a solution of <strong>[52764-11-1]2,6-dichloropyridin-3-ol</strong> (16.3 g, 0.1 mol) and K2C03 (41.4 g, 0.3 mol) in DMF (200 mL) were added Mel (21.3 g, 0.15 mol). The mixture was allowed to stir at 80 C for 2 hours. The mixture was then diluted with water (200 mL) and extracted with EtOAc (200 mL x 3). The organic layer was washed with brine (200 mL x 3), dried over Na2S04, filtered and the solvent was concentrated in vacuo to provide 2,6-dichloro-3-methoxypyridine (17.0 g, yield: 96.0%). 1H- MR (CDC13; 400 MHz) delta 7.12-7.18 (m, 2H), 3.86 (s, 3H). MS (M+H)+: 178 / 180 / 182.
96% With potassium carbonate; In N,N-dimethyl-formamide; at 80℃; for 2h; Step 2-Synthesis of 2,6-dichloro-3-methoxypyridine To a solution of <strong>[52764-11-1]2,6-dichloropyridin-3-ol</strong> (16.3 g, 0.1 mol) and K2CO3 (41.4 g, 0.3 mol) in DMF (200 mL) were added MeI (21.3 g, 0.15 mol). The mixture was allowed to stir at 80 C. for 2 hours. The mixture was then diluted with water (200 mL) and extracted with EtOAc (200 mL*3). The organic layer was washed with brine (200 mL*3), dried over Na2SO4, filtered and the solvent was concentrated in vacuo to provide 2,6-dichloro-3-methoxypyridine (17.0 g, yield: 96.0%). 1H-NMR (CDCl3, 400 MHz) delta 7.12?7.18 (m, 2H), 3.86 (s, 3H). MS (M+H)+: 178/180/182.
 

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