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Chemical Structure| 1104606-44-1 Chemical Structure| 1104606-44-1

Structure of 1104606-44-1

Chemical Structure| 1104606-44-1

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Product Details of [ 1104606-44-1 ]

CAS No. :1104606-44-1
Formula : C7H5ClFNO
M.W : 173.57
SMILES Code : FC1=CN=C(C(CCl)=O)C=C1
MDL No. :MFCD17169899

Safety of [ 1104606-44-1 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H311-H331-H341
Precautionary Statements:P201-P202-P261-P264-P270-P271-P280-P302+P352-P304+P340-P308+P313-P310-P330-P361-P403+P233-P405-P501
Class:6.1
UN#:2810
Packing Group:

Application In Synthesis of [ 1104606-44-1 ]

* 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 [ 1104606-44-1 ]

[ 1104606-44-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 41404-58-4 ]
  • [ 67442-07-3 ]
  • [ 1104606-44-1 ]
YieldReaction ConditionsOperation in experiment
Step A: 2-Chloroacetyl-5-fluoropyridine. 2-Bromo-5-fluoropyridine (50.0 g, 284 mmol) in 200 mL of THF was added drop-wise over 25 min to isopropylmagnesium chloride (2 M in THF, 284 mL, 568 mmol) at RT, and the mixture was stirred for 2 hours at room temperature. A solution of <strong>[67442-07-3]2-chloro-N-methoxy-N-methylacetamide</strong> in 150 mL of THF was added dropwise over 30 minutes to the reaction mixture at RT. The mixture was stirred at RT overnight. The mixture was then poured into 2000 g of ice with 500 mL of 2 N HCl. The mixture was extracted into ether, washed with brine, dried over anhydrous sodium sulfate and concentrated to a residue, which was dissolved in 1 L of warm hexane and treated with several grams of silica gel to remove colored impurities. The mixture was then filtered. The filtrate was concentrated and chilled at ice temperature for 30 minutes. The resulting solid was isolated by filtration to give 2-chloroacetyl-5-fluoropyridine. 1H NMR (500 MHz, CDCl3): delta 8.53 (d, 1H), 8.19 (dd, 1H), 7.60 (td, 1H), 5.09 (s, 2H).
Example 50a2-Chloro-1-(5-fluoro-2-pyridyl)ethanone2-Bromo-5-fluoropyridine (3.88 g, 22 mmol) dissolved in toluene (10 mL) was added slowly to a solution of isopropylmagnesium chloride (13.2 mL, 26.4 mmol, 2M in THF) in toluene (30 mL) at room temperature.The reaction mixture was stirred for 3.5 hours at room temperature, cooled to 0° C. and a solution of <strong>[67442-07-3]2-chloro-N-methoxy-N-methyl-acetamide</strong> (3.64 g, 26.4 mmol) in toluene (10 mL) was added slowly.The reaction mixture was stirred for 2.5 hours at 0° C., quenched with saturated ammonium chloride, diluted with ethyl acetate and saturated sodium bicarbonate and extracted with ethyl acetate (2*100 mL).The combined extracts were dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to afford 3.75 g (98percent) of the title compound which was used in the next step without further purification. 1H NMR (400 MHz, CDCl3) delta ppm 5.07 (s, 2H), 7.56 (td, 1H), 8.17 (dd, 1H), 8.50 (d, 1H).
Step A: 2-ChIoroacetyl-5-fluoropyridine.2-Bromo-5-fluoropyridine (50.0 g, 284 mmol) in 200 mL of THF was added dropwise over 25 min to isopropylmagnesium chloride (2 M in THF, 284 mL, 568 mmol) at RT, and the mixture was stirred for 2 hours at room temperature. A solution of 2-chloro-N-methoxy-N- methylacetamide (43.0 g, 313 mmol) in 150 mL of THF was added dropwise over 30 minutes to the reaction mixture at RT. The mixture was stirred at RT overnight. The mixture was then poured into 2000 g of ice with 500 mL of 2 N HCl. The mixture was extracted into ether, washed with brine, dried over anhydrous sodium sulfate and concentrated. The resulting residue was dissolved in 1 L of warm hexane and treated with several grams of silica gel to remove colored impurities. The resulting mixture was then filtered, and the filtrate was concentrated and chilled in an ice bath for 30 minutes. The resulting solid was isolated by filtration to give 2-chloroacetyl- 5-fluoropyridine. 1HNMR (500 MHz, CDCI3): 6 8.53 (d, 1 H), 8.19 (dd, 1 H), 7.60 (td, 1 H), 5.09 (s, 2 H).
 

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