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Chemical Structure| 34859-78-4 Chemical Structure| 34859-78-4

Structure of 34859-78-4

Chemical Structure| 34859-78-4

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Product Details of [ 34859-78-4 ]

CAS No. :34859-78-4
Formula : C13H8F3NO3
M.W : 283.20
SMILES Code : [O-][N+](=O)C1=CC=C(OC2=CC=C(C=C2)C(F)(F)F)C=C1

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Application In Synthesis of [ 34859-78-4 ]

* 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 [ 34859-78-4 ]

[ 34859-78-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 34859-78-4 ]
  • [ 57478-19-0 ]
YieldReaction ConditionsOperation in experiment
81% With palladium on activated charcoal; hydrogen; In methanol; at 20℃; for 15h; To 1-nitro-4-(4-(trifluoromethyl)phenoxy)benzene (865 mg, 3.06 mmol), dissolved in MeOH(15 mL), was added Pd/C (100 mg). After the reaction mixture was stirred at ambienttemperature for 15 h, under hydrogen atmosphere (hydrogen gas in a balloon), it was filteredthrough a pad of Celite to remove Pd/C residue. The volatiles were removed in vacuo and theresulting solid triturated with DCM (1 mL) and hexanes (15 mL). 4-(4-(trifluoromethyl)phenoxy)aniline was isolated as a solid (720 mg, 81%). M.P: 70-71 C (lit.73-74 C4); 1H NMR (CDCl3, 500 MHz): 7.53 (d, J = 8.0 Hz, 2H), 6.98 (d, J = 8.0 Hz, 2H),6.89 (d, J = 8.0 Hz, 2H), 6.72 (d, J = 8.0 Hz, 2H).
With hydrogen;5% Pd(II)/C(eggshell); In methanol; under 760.051 - 1520.1 Torr;Inert atmosphere; In a hydrogenation bottle, crude (3) was dissolved in MeOH; solution was purged with N2 prior to the addition of 50- 100 mg of 5 wt % Pd on activated carbon. The reaction mixture was placed in a hydrogenator and shaken with 1-2 atm H2 for 1-2 hr. Upon completion of the reaction, the catalyst was filtered through the fritted funnel and was rinsed with MeOH. MeOH was evaporated using the rotary evaporator to give the final crude product (4). (Approx. 80 % yield).
 

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