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Chemical Structure| 433926-47-7 Chemical Structure| 433926-47-7

Structure of 433926-47-7

Chemical Structure| 433926-47-7

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Product Details of [ 433926-47-7 ]

CAS No. :433926-47-7
Formula : C8H6ClF3O2
M.W : 226.58
SMILES Code : FC(F)(F)OC1=CC(Cl)=CC(CO)=C1
MDL No. :MFCD06660310

Safety of [ 433926-47-7 ]

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 [ 433926-47-7 ]

* 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 [ 433926-47-7 ]

[ 433926-47-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 433926-46-6 ]
  • [ 433926-47-7 ]
YieldReaction ConditionsOperation in experiment
100% To a solution of 3-chloro-5-trifluoromethoxybenzoic acid (22.5 g, 93.5 mmol; see step (iv) above) in anhydrous THF (1200 mL) under a N2 atmosphere at room temperature was added a solution of BH3.THF complex (140 mL of 1M in THF; 140.3 mmol). The solution was refluxed for 2 h, cooled to room temperature and stirred for 18 hours, quenched cautiously with H2O and concentrated in vacuo to remove most of the THF. The residue was diluted with EtOAc and the organics were washed with brine (3*), dried (Na2SO4), filtered and concentrated in vacuo to give the crude sub-title compound (21.2 g, 100%) as an oil that was used without further purification. 1H NMR (300 MHz, CDCl3): δ7.33 (s, 1H), 7.17 (s, 1H), 7.14 (s, 1H), 4.72 (s, 2H), 2.05 (br s, 1H)
100% With borane-THF; In tetrahydrofuran; at 20℃; for 20h;Heating / reflux; To a solution of 3-chloro-5-trifluoromethoxybenzoic acid (22.5 g, 93.5 mmol; see step (iv) above) in anhydrous THF (1200 mL) under a N2 atmosphere at room temperature was added a solution of [BH3THF] complex (140 mL of 1M in THF; 140.3 mmol). The solution was refluxed for 2 h, cooled to room temperature and stirred for 18 hours, quenched cautiously with [HZO] and concentrated in vacuo to remove most of the THF. The residue was diluted with EtOAc and the organics were washed with brine (3x), dried [(NA2SO4),] filtered and concentrated in vacuo to give the crude sub-title compound (21.2 g, [100%)] as an oil that was used without further purification. 'H NMR (300 MHz, [CDCI3)] : A 7.33 (s, 1H), 7.17 (s, 1H), 7.14 (s, 1H), 4.72 (s, 2H), 2.05 [(BRS, 1H)]
 

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