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Chemical Structure| 1256821-01-8 Chemical Structure| 1256821-01-8

Structure of 1256821-01-8

Chemical Structure| 1256821-01-8

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Product Details of [ 1256821-01-8 ]

CAS No. :1256821-01-8
Formula : C8H7F2NO
M.W : 171.15
SMILES Code : CC(C1=CC=C(C(F)F)N=C1)=O
MDL No. :MFCD18256461

Safety of [ 1256821-01-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 1256821-01-8 ]

* 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 [ 1256821-01-8 ]

[ 1256821-01-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 845827-13-6 ]
  • [ 97674-02-7 ]
  • [ 1256821-01-8 ]
YieldReaction ConditionsOperation in experiment
87% To a degassed solution of <strong>[845827-13-6]5-bromo-2-(difluoromethyl)pyridine</strong> (1 g, 4.81 mmol) and tributyl(1-ethoxyethenyl)stannane (1.95 mL, 5.77 mmol) in DMF (20 mL) under N2 was added PdCI2(PPh3)2 (34 mg, 0.05 mmol). The reaction was stirred at 100 C for 2.5 h. The reaction mixture was diluted with ether (40 mL) and treated with aqueous KF solution (1.4 g of KF in 40 mL water). The mixture was stirredvigorously for 1 h before being filtered through Celite. The filtrate was diluted with ethyl acetate (50 mL), washed with saturated sodium bicarbonate solution, then brine, dried over MgSO4, filtered and concentrated under reduced pressure. The crude material was suspended in THF (20 mL) and 2M HCI (20 mL) was added. The solution was stirred vigorously for 1 5 minutes at RT before being concentratedto remove THF, then extracted with DCM (3 x 50 mL). The combined organics were dried over MgSO4, filtered and concentrated under reduced pressure. The crude material was purified by Biotage Isolera chromatography (silica gel, eluting with heptane-EtOAc, 1:0 to 4:1) to afford 730mg (87% yield) of the title compound as a colourless oil.1H NMR (500MHz, DMSO-d6): 6 [ppm] 9.20 (d, J = 1.6 Hz, 1H), 8.47 (dd, J = 8.1, 2.1 Hz, 1H), 7.86 (d, J = 8.1 Hz, 1H), 7.05 (t, J = 54.6 Hz, 1H), 2.67 (5, 3H).LCMS (Analytical Method A) Rt = 0.94 mm, MS (ESIpos): m/z = 171 .9 (M+H).
68% With tetrakis(triphenylphosphine) palladium(0); In 1,4-dioxane; at 100℃; for 2h; Into a 500-mL 4-necked round-bottom flask, was placed a solution of 5-bromo-2- (difluoromethyl)pyridine (18 g, 86.54 mmol, 1.00 equiv) in dioxane (180 mL), tributyl(iethoxyethenyl)stannane (35 g, 96.91 mmol, 1 .12 equiv), tetrakis(triphenylphosphane) palladium (3 g, 2.60 mmol, 0.03 equiv). The resulting solution was stirred for 2 h at 1 00CC. The reaction mixture was cooled with a water bath. The reaction was then quenched by theaddition of 250 mL of (2N) HCI. The pH value of the solution was adjusted to 8 with sodium carbonate (2 mol/L). The resulting solution was extracted with 3x500 mL of ethyl acetate andthe organic layers were combined. The resulting mixture was washed with 1x200 mL of H20. The resulting mixture was washed with 1x200 mL of brine. The mixture was dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:10). This resulted in lOg (68%) of 1-[6-(difluoromethyl)pyridin-3-yl]ethan-1 -one as yellow oil.
68% With tetrakis(triphenylphosphine) palladium(0); In 1,4-dioxane; at 100℃; for 2h; Into a 500-mL 4-necked round-bottom flask, was placed a solution of 5-bromo-2- (difluoromethyl)pyridine (18 g, 86.54 mmol, 1.00 equiv) in dioxane (180 ml_), tributyl(1- ethoxyethenyl)stannane (35 g, 96.91 mmol, 1.12 equiv), tetrakis(triphenylphosphane) palladium (3 g, 2.60 mmol, 0.03 equiv). The resulting solution was stirred for 2 h at 100C. The reaction mixture was cooled with a water bath. The reaction was then quenched by the addition of 250 ml. of (2N) HCI. The pH value of the solution was adjusted to 8 with sodium carbonate (2 mol/L). The resulting solution was extracted with 3x500 mL of ethyl acetate and the organic layers were combined. The resulting mixture was washed with 1x200 mL of water. The resulting mixture was washed with 1x200 mL of brine. The mixture was dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 :10). This resulted in 10 g (68%) of 1-[6- (difluoromethyl)pyridin-3-yl]ethan-1-one as yellow oil.
 

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