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Chemical Structure| 851314-55-1 Chemical Structure| 851314-55-1

Structure of 851314-55-1

Chemical Structure| 851314-55-1

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Product Details of [ 851314-55-1 ]

CAS No. :851314-55-1
Formula : C17H23F2NO4
M.W : 343.37
SMILES Code : O=C(OCC)C(F)(F)CN(CC1=CC=CC=C1)CCC(OCC)=O
MDL No. :MFCD18433564

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Application In Synthesis of [ 851314-55-1 ]

* 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 [ 851314-55-1 ]

[ 851314-55-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 851314-55-1 ]
  • [ 1067915-34-7 ]
YieldReaction ConditionsOperation in experiment
81% With n-butyllithium; diisopropylamine; In tetrahydrofuran; hexane; at -78℃; To a solution of diisopropylamine (2.08 mL, 14.9 mmol) in THF (150 mL) under nitrogen and at-78C, was added BuLi (1.6 M in hexane, 8.52 mL, 13.64 mmol), followed 45 min later by compound W (2.13 g, 6.2 mmol) in THF (50 mL). The cooling bath was removed and the reaction mixture warmed up slowly overnight. Sat. aq. NH4CI (200 mL) was added and the layers were separated. The aqueous phase was extracted with EtOAc (3x150 mL). The combined organic layers were washed with brine and dried over Na2S04. Purification of the residue by FC (EtOAc/heptane 1: 9) gave the title compound (1.5 g, 81 %). LC-MS: Rut-1. 04 min, ES+ = 298.22.
With potassium tert-butylate; In tetrahydrofuran; at 0 - 20℃; for 1h; 10243] To a solution of compoundS (8.0 g, 23.2 mmol) inTHF (200 mE) was added t-l3uOK (3.90 g, 34.9 mmol) slowlyunder 0 C. Then the mixture was stirred at rt for 1 hout Themixture was quenched with water and extracted by EtOAc(100 mE). The organic layer was dried over Na2SO4 andconcentrated in vacuum to give the crude product compound6. ECMS: 298 [M+1].
With lithium hexamethyldisilazane; In tetrahydrofuran; at 0 - 3℃; for 3h;Large scale; [0155] To a solution of ethyl 3-(benzyl(3-ethoxy-3-oxopropyl)amino)-2,2-difluoropropa noate (2.25 kg, 6.55 mol) in dry THF (11.5 L) at 0C was added lithium hexamethyldisilazide in THF (11.0 kg, 20%, 13.1 mol) dropwise, maintaining the temperature below 3 C. The reaction mixture was stirred for 3 hours. After cornpetion of the reaction, the reaction rnxture was extracted three times with saturated sodium choride so?ution and the aqueous ayer was back extracted once with EtOAc. The combined organic phases were dried over sodium sufate and concentrated in vacuo to give the tit?e compound as a reddish oi (2066 g). This crude product was used in the next step without further purification. MS (ESl) calcd forC15H17F2N03: 297.1; found: 298.1 [M+H]. 1H NMR (400 MHz, CDCI3) 6 7.32-7.28 (m, 5H), 4.06(q, J = 7.2Hz, 2H), 3.76-3.72 (m, 1H), 3.65 (s, 2 H), 3.30 (s, 2H), 2.82 (t, J = 12.4Hz, 2H), 1.17 (t, J = 7.2Hz, 2H).
  • 2
  • [ 851314-55-1 ]
  • [ 1209780-71-1 ]
 

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