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Chemical Structure| 207994-09-0 Chemical Structure| 207994-09-0

Structure of 207994-09-0

Chemical Structure| 207994-09-0

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Product Details of [ 207994-09-0 ]

CAS No. :207994-09-0
Formula : C6H2Cl2FNO
M.W : 193.99
SMILES Code : O=C(Cl)C1=NC=C(Cl)C=C1F

Safety of [ 207994-09-0 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P321-P363-P405-P501
Class:8
UN#:3265
Packing Group:

Application In Synthesis of [ 207994-09-0 ]

* 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 [ 207994-09-0 ]

[ 207994-09-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 207994-08-9 ]
  • [ 207994-09-0 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride; In hexane; toluene; Example H6 3-Fluoro-5-chloro-2-pyridinecarbonyl chloride 71.38 g of <strong>[207994-08-9]3-fluoro-5-chloro-2-pyridinecarboxylic acid</strong> is initially introduced into a round-bottomed flask and heated up to 90 C. 59 ml of thionyl chloride are added dropwise from a dropping funnel in the course of 30 minutes, and the gas formed is passed into sodium hydroxide solution. The mixture is subsequently stirred at 100 C. for a further 5 hours. The thionyl chloride is then distilled off under normal pressure. After addition of 50 ml of dry toluene, 20 ml thereof are distilled off. The solution thus obtained is poured onto 200 ml of n-hexane and the mixture is stirred overnight. After cooling in an ice-bath, the mixture is filtered and the material on the filter is washed twice with n-hexane. 68.7 9 of the desired compound are obtained as a brown solid. 1H-NMR (CDCl3): 8.60 ppm (d, 1H); 7.69 ppm (dxd, 1H).
In thionyl chloride; hexane; toluene; Example P6 3-Fluoro-5-chloro-2-pyridinecarboxylic Acid Chloride 71.38 g of <strong>[207994-08-9]3-fluoro-5-chloro-2-pyridinecarboxylic acid</strong> (Example P4) are placed in a round-bottomed flask and heated to 90 C. 59 ml of thionyl chloride are added dropwise from a dropping funnel over a period of 30 minutes, and the gas formed is introduced into sodium hydroxide solution. Stirring is then carried out for 5 hours at 100 C., after which the thionyl chloride is distilled off at normal pressure. After the addition of 50 ml of dry toluene, 20 ml thereof are distilled off. The resulting solution is poured into 200 ml of n-hexane and stirred overnight. After cooling in an ice-bath, the mixture is filtered and the filtration residue is washed twice with n-hexane. 68.7 g of the desired compound are obtained in the form of a brown solid. 1H-NMR (CDCl3): 8.60 ppm (d, 1H); 7.69 ppm (dxd, 1H).
 

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