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Chemical Structure| 536975-35-6 Chemical Structure| 536975-35-6

Structure of 536975-35-6

Chemical Structure| 536975-35-6

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Product Details of [ 536975-35-6 ]

CAS No. :536975-35-6
Formula : C15H11F3O3
M.W : 296.24
SMILES Code : OC(=O)C1=CC=C(OCC2=CC=CC=C2)C(=C1)C(F)(F)F
MDL No. :MFCD12405653

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Application In Synthesis of [ 536975-35-6 ]

* 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 [ 536975-35-6 ]

[ 536975-35-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 67515-55-3 ]
  • [ 100-51-6 ]
  • [ 536975-35-6 ]
YieldReaction ConditionsOperation in experiment
72% 4-Benzyloxy-3-trifluoromethyl-benzoic Acid (CAB03046) Sodium hydride (60%, 1.80 g, 45 mmol) was added to a solution of <strong>[67515-55-3]4-fluoro-3-trifluoromethyl benzoic acid</strong> (4.162 g, 20 mmol) and benzyl alcohol (3.25 g, 30 mmol) in DMSO (50 mL). The mixture was stirred overnight at room temperature, poured into water (50 mL) and acidified with concentrated hydrochloric acid. The white precipitate was filtered off, dissolved in ethyl acetate (ca. 50 mL), dried over sodium sulphate and concentrated under reduced pressure. The residue was recrystallized from ethyl acetate/hexane. Yield: 4.252 g (72%). 1H-NMR (400 MHz, CDCl3) delta=5.37 (s, 2H), 7.32-7.48 (m, 6H), 8.12 (d, J=2.0 Hz, 1H), 8.18 (dd, J=8.6, 2.0 Hz, 1H), 13.16 (br s, 1H, -COOH). LRMS (FAB+): 91.1 (100), 297.1(18, [M+H]+).
(93-1) Synthesis of 4-benzyloxy-3-trifluoromethylbenzoic acid (compound 93-1) To a solution of potassium t-butoxide (27.5 g) in N,N-dimethylformamide (120 ml) was added dropwise a solution of benzyl alcohol (15.9 ml) in N,N-dimethylformamide (60 ml) over 10 min. The mixture was stirred for 30 min, and a solution of <strong>[67515-55-3]4-fluoro-3-trifluoromethylbenzoic acid</strong> (20.0 g) in N,N-dimethylformamide (90 ml) was added under ice-cooling. The mixture was stirred at room temperature for 1 hr, and further at 50C for 1 hr. The reaction mixture was added to ice water, and acidified with 1M hydrochloric acid (300 ml). The precipitated solid was collected by filtration, and washed with water and then hexane to give the object product (28.2 g) as a white powder. 1H-NMR(CDCl3) delta (ppm): 5.29(2H, s), 7.10(1H, d, J=8.7Hz), 7.33-7.37(1H, m), 7.39-7.45(4H, m), 8.22(1H, dd, J=2.0, 8.7Hz), 8.36(1H, d, J=2.0Hz).
 

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