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Chemical Structure| 163769-73-1 Chemical Structure| 163769-73-1

Structure of 163769-73-1

Chemical Structure| 163769-73-1

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Product Details of [ 163769-73-1 ]

CAS No. :163769-73-1
Formula : C4H3Cl3N2
M.W : 185.44
SMILES Code : ClC(C1=NC=CN1)(Cl)Cl
MDL No. :MFCD18450232

Safety of [ 163769-73-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H319
Precautionary Statements:P305+P351+P338

Application In Synthesis of [ 163769-73-1 ]

* 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 [ 163769-73-1 ]

[ 163769-73-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 64-17-5 ]
  • [ 163769-73-1 ]
  • [ 33543-78-1 ]
YieldReaction ConditionsOperation in experiment
64.3% With sulfuric acid; at 20℃;Reflux; The above-obtained residue was dissolved in EtOH (300 mL). To this solution, cone. H2S04 (98percent, 30 mL, 522 mmol, 2.76 eq) was added dropwise while keeping the reaction temperature below 25 °C. The resulting mixture was stirred at reflux for 7 h and then stirred at RT overnight. The mixture was concentrated in vacuo to remove EtOH. The resulting suspension was diluted with ice -water (200 mL) and neutralized with concentrated ammonium hydroxide to adjust the pH to 5-6 while keeping the temperature below 5 °C. The solid was collected by filtration, rinsed with water (10 mL x 3), and dried in vacuo to afford the first batch of crude product (10 g). The filtrate was extracted with ethyl acetate (200 mL x 2). The combined organic layer was washed with brine, dried over Na2S04 and filtered. The filtrate was concentrated in vacuo. The resulting residue was combined with the first batch crude product and then re-crystallized in isopropyl ether to afford ethyl lH-imidazole- 2-carboxylate (18 g, 64.3percent yield ).
The above-obtained residue (C-2) is dissolved in EtOH (300 mL). To this solution, cone. H2S04 (98percent, 30 mL, 522 mmol, 2.76 eq) is added dropwise while keeping the reaction temperature below 25 °C. The resulting mixture is stirred at reflux for 7 h and then stirred at RT overnight. The mixture is concentrated in vacuo to remove EtOH. The resulting suspension is diluted with ice-water (200 mL) and neutralized with concentrated ammonium hydroxide to adjust the pH to 5-6 while keeping the temperature below 5 °C. The solid is collected by filtration, rinsed with water (10 mL x 3), and dried in vacuo to afford a first portion of the product. The filtrate is extracted with ethyl acetate (200 mL x 2). The combined organic layers are washed with brine, dried over Na2S04 and filtered. The filtrate is concentrated in vacuo. The resulting residue is combined with the first portion of product and then recrystallized in isopropyl ether to afford the product, ethyl lH-imidazole-2-carboxylate (C-3).
 

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