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Chemical Structure| 207799-86-8

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Product Details of [ 207799-86-8 ]

CAS No. :207799-86-8
Formula : C8H7ClF2O
M.W : 192.59
SMILES Code : OCC(F)(F)C1=CC=C(Cl)C=C1
MDL No. :MFCD28038847

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Application In Synthesis of [ 207799-86-8 ]

* 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 [ 207799-86-8 ]

[ 207799-86-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 130754-19-7 ]
  • [ 207799-86-8 ]
YieldReaction ConditionsOperation in experiment
95% With sodium tetrahydroborate; ethanol; at 20℃; for 0.5h; To a stirred solution of ethyl 2(4chiorophenyTh22difluoroacetate (6.7 g, 29 mmoi) in EtOH (1 0 mLj wa added NaBH4 (1 S5 g 41 mmol) at toom temperature The susptnsion was slowly transformed tO a clear solution. After stirring for 30mm at rt. the: ester was consumed. The reaction mixture wa.s quenched with aqueous IN HG under icewater bath cooling The mixturc %JS ttrctcttd with EtOAc [he organic phasts were washed w nh biuie dried O et Na2SO4 aim concentmted to attoid the title compound as s colni less liquid iS S) 95%). 11 NMR (400 MHz C 003) ii 7.46 (d. qi 8 Hz, 2.1:1). 7.42 (d.. J::; 8.8 Hz. 211), 3.95 (tJ 13.1 Hz,ZH).
With sodium hydroxide; In diethyl ether; water; Step A Synthesis of 2,2-difluoro-2-(4-chlorophenyl)ethanol as an intermediate Lithium aluminum hydride, 2.4 grams (0.063 mole), is placed in a reaction vessel, and 200 mL of diethyl ether is added dropwise with stirring. To this is added dropwise a solution of 22.8 grams (0.097 mole) of <strong>[130754-19-7]ethyl 4-chlorophenyldifluoroacetate</strong> (prepared by methods taught by W. J. Middleton et al., J. Org. Chem., (1980), 45, 2883-2887) in 100 mL of diethyl ether, while maintaining the reaction mixture temperature at about 25 C. Upon completion of addition, the reaction mixture is stirred at ambient temperature for about 36 hours. The reaction is then quenched by the careful dropwise addition of an aqueous solution of 10% sodium hydroxide. The reaction mixture is slowly made acidic with aqueous 2N hydrochloric acid and then is diluted with 200 mL of water. The organic layer is separated, and the aqueous layer is washed with two 300 mL portions of diethyl ether. The organic layer and the diethyl ether washes are combined and washed with one 250 mL portion of an aqueous solution saturated with sodium chloride. The organic layer is dried with magnesium sulfate and filtered. The filtrate is concentrated under reduced pressure, yielding 2,2-difluoro-2-(4-chlorophenyl)ethanol.
 

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