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[ CAS No. 77544-60-6 ] {[proInfo.proName]}

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Chemical Structure| 77544-60-6
Chemical Structure| 77544-60-6
Structure of 77544-60-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 77544-60-6 ]

CAS No. :77544-60-6 MDL No. :MFCD22056303
Formula : C15H24O7S Boiling Point : -
Linear Structure Formula :C7H7SO3(CH2CH2O)4H InChI Key :FGDJUEZBMFELRW-UHFFFAOYSA-N
M.W : 348.41 Pubchem ID :13456094
Synonyms :
Chemical Name :2-(2-(2-(2-Hydroxyethoxy)ethoxy)ethoxy)ethyl 4-methylbenzenesulfonate

Safety of [ 77544-60-6 ]

Signal Word:Danger Class:6.1,8
Precautionary Statements:P280-P301+P310-P305+P351+P338-P310 UN#:2927
Hazard Statements:H301-H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 77544-60-6 ]

* 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 [ 77544-60-6 ]

[ 77544-60-6 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 19362-77-7 ]
  • [ 77544-60-6 ]
  • 2-{2-[2-(2-{4-[4-(2-{2-[2-(2-Hydroxy-ethoxy)-ethoxy]-ethoxy}-ethylsulfanyl)-phenylsulfanyl]-phenylsulfanyl}-ethoxy)-ethoxy]-ethoxy}-ethanol [ No CAS ]
  • 2
  • [ 24782-43-2 ]
  • [ 77544-60-6 ]
  • ethyl 4-(2-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)ethoxy)quinoline-2-carboxylate [ No CAS ]
  • 3
  • [ 349-58-6 ]
  • [ 77544-60-6 ]
  • C16H20F6O5 [ No CAS ]
YieldReaction ConditionsOperation in experiment
63% With potassium carbonate; In N,N-dimethyl-formamide; at 50℃; for 15h;Inert atmosphere; To a 100-mL two-neck eggplant-shaped flask, 2,4- bis (trifluoromethyl) phenol (230 mg, 1 mmol, 1 eq) , potassium carbonate (346 mg, 2.5 mmol, 2.5 eq, baked at 300°C for 2 to 3 h) , and 3 mL of dry dimethylformamide were added. Then, 2 mL of dry dimethylformamide of the compound D-I (418 mg, 1.2 mmol, 1.2 eq) was gradually added thereto in an argon atmosphere. The mixture was stirred at room temperature for 2 hours and at 50°C for 13 hours. The reaction was followed by TLC (Sitheta2/EtOAc : Hexane = 1 : 1) and completed when the production of the compound of interest (Rf value: 0.4) and the exhaustion of the raw materials (phenol, Rf value: 0.9) were confirmed. The solvents were distilled off under reduced pressure using a vacuum pump. After the addition of ethyl acetate (approximately 300 mL) , the organic phase was washed with an aqueous saturated citric acid solution (100 mL, three times) and with a saturated saline (100 mL, twice) . The organic phase was dried over anhydrous magnesium sulfate. Insoluble matter was filtered off. Then, the solvents were distilled off under reduced pressure. The residue was vacuum-dried to obtain a white solid. The solid was purified by column chromatography (SiO2/ (second) EtOAc :Hexane = 1 : 1 - 4 : 1) . The solvents were distilled off under reduced pressure. The residue was vacuum- dried to obtain a pale yellow oil. Identification was conducted by 1H-NMR.Experimental Results>Pale Yellow OilYield: 252 mg (63percent)
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