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[ CAS No. 140690-56-8 ] {[proInfo.proName]}

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Chemical Structure| 140690-56-8
Chemical Structure| 140690-56-8
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Product Details of [ 140690-56-8 ]

CAS No. :140690-56-8 MDL No. :MFCD00010306
Formula : C9H5BrF6 Boiling Point : -
Linear Structure Formula :- InChI Key :SWFFFUJOWAJJCH-UHFFFAOYSA-N
M.W : 307.03 Pubchem ID :518871
Synonyms :

Safety of [ 140690-56-8 ]

Signal Word:Danger Class:8,3
Precautionary Statements:P280-P305+P351+P338-P310 UN#:2920
Hazard Statements:H225-H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 140690-56-8 ]

* 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 [ 140690-56-8 ]

[ 140690-56-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 66495-88-3 ]
  • [ 140690-56-8 ]
  • [ 1264753-89-0 ]
YieldReaction ConditionsOperation in experiment
91% Reference Example 53 3-[2,4-bis(trifluoromethyl)benzyl]oxy}-2-methoxybenzaldehyde; [Show Image] To a solution (16 mL) of <strong>[66495-88-3]3-hydroxy-2-methoxybenzaldehyde</strong> (1.00 g) in N,N-dimethylformamide was added potassium carbonate (1.37 g), and the mixture was stirred at room temperature for 0.5 hr. To the reaction mixture was added a solution (2 mL) of 1-(bromomethyl)-2,4-bis(trifluoromethyl)benzene (2.29 g) in N,N-dimethylformamide, and the mixture was stirred at room temperature for 3 days. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=100:0→90:10) to give the title compound as a pale-yellow oil (yield: 2.27 g, 91%). 1H-NMR (DMSO-d6, 300 MHz):δ3.92 (3H, s), 5.44 (2H, s), 7.20-7.29 (1H, m), 7.36 (1H, dd, J = 7.9, 1.6 Hz), 7.49 (1H, dd, J = 8.0, 1.6 Hz), 8.10 (1H, d, J = 8.3 Hz), 8.14 (1H, s), 8.20 (1H, d, J = 8.3 Hz), 10.32 (1H, s).
  • 2
  • [ 436-77-1 ]
  • [ 140690-56-8 ]
  • C46H44F6N2O6*2HI [ No CAS ]
YieldReaction ConditionsOperation in experiment
5.1 g Weigh 6.10g of <strong>[436-77-1]fangchinoline</strong> dissolved in 100mL of dichloromethaneIn a 500 mL three-necked flask,Add diethylamine10 mL, 2,4-bis(trifluoromethyl)benzyl bromide 3.10 g,Stirring, heat-reacting at 60 C for 12 h, TLC detection of anti-chinolineReaction, distill off dichloromethane, cool to room temperature, neutralize to neutral with 10% hydrobromic acid, dissolve with 200 mL of water, and use 500 g of Treatment with H-type 732 cationic resin, washing with water and then eluting with dilute ammonia water, collecting the fractions containing the product, and steaming under reduced pressure to the liquid volumeAbout 50mL, crystallized at room temperature overnight, filtered, TLC tracking reaction and product separation and purification process, solids dried at 60 C4h, the product was obtained as a yellow powder, 5.10g.
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Technical Information

? Acyl Group Substitution ? Alkyl Halide Occurrence ? Appel Reaction ? Benzylic Oxidation ? Birch Reduction ? Blanc Chloromethylation ? Bouveault-Blanc Reduction ? Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions ? Catalytic Hydrogenation ? Chan-Lam Coupling Reaction ? Chugaev Reaction ? Complex Metal Hydride Reductions ? Corey-Kim Oxidation ? Dess-Martin Oxidation ? Epoxidation ? Ester Cleavage ? Friedel-Crafts Reaction ? General Reactivity ? Grignard Reaction ? Halogenation ? Heat of Combustion ? Hiyama Cross-Coupling Reaction ? Hydride Reductions ? Hydrogenolysis of Benzyl Ether ? Jones Oxidation ? Kinetics of Alkyl Halides ? Kumada Cross-Coupling Reaction ? Lawesson's Reagent ? Leuckart-Wallach Reaction ? Mannich Reaction ? Martin's Sulfurane Dehydrating Reagent ? Mitsunobu Reaction ? Moffatt Oxidation ? Nomenclature of Ethers ? Nucleophilicity of Organophosphorus Compounds ? Organophosphorus Compounds as Reducing Agents ? Oxidation of Alcohols by DMSO ? Oxidation States of Organophosphorus Compounds ? Petasis Reaction ? Preparation of Alcohols ? Preparation of Alkylbenzene ? Preparation of Amines ? Preparation of Ethers ? Reactions of Alcohols ? Reactions of Alkyl Halides with Reducing Metals ? Reactions of Amines ? Reactions of Benzene and Substituted Benzenes ? Reactions of Dihalides ? Reactions of Epoxides ? Reactions of Ethers ? Reactions of Phosphorus and Sulfur Ylides ? Reactions with Organometallic Reagents ? Ritter Reaction ? Sharpless Olefin Synthesis ? Specialized Acylation Reagents-Carbodiimides and Related Reagents ? Specialized Acylation Reagents-Ketenes ? Specialized Acylation Reagents-Vilsmeier Reagent ? Stille Coupling ? Substitution and Elimination Reactions of Alkyl Halides ? Suzuki Coupling ? Swern Oxidation ? Ugi Reaction ? Vilsmeier-Haack Reaction
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