Specialty Chemicals
  • BIS(2,2,2-TRIFLUOROETHYL) ETHER

    • Product Name   :   

      BIS(2,2,2-TRIFLUOROETHYL) ETHER

    • CAS No   :   

      333-36-8

    • Project State   :   

      Commercial

    General Description

    Buy cost-effective 99% pure BIS(2,2,2-TRIFLUOROETHYL) ETHER 333-36-8 now

    • Molecular Formula:C4H4 F6 O
    • Molecular Weight:182.066
    • Appearance/Colour:clear colorless liquid 
    • Vapor Pressure:180mmHg at 25°C 
    • Melting Point:25°C 
    • Refractive Index:n20/D 1.300(lit.) 
    • Boiling Point:63.9°Cat760mmHg 
    • Flash Point:1.7°C 
    • PSA:9.23000 
    • Density:1.361g/cm3 
    • LogP:2.12760 

    BIS(2,2,2-TRIFLUOROETHYL) ETHER(Cas 333-36-8) Usage

    Manufacturing Process

    23 parts of sodium metal were placed in 300 parts of dry dioxane in a reactor equipped with an agitator and reflux condenser. The dioxane was heated to reflux while stirring.150 parts of 2,2,2-trifluoroethanol were added very slowly in the period of about 1 hour, or until the sodium was all reacted, to form sodium 2,2,2-trifluoroethylate. 250 parts of 2,2,2-trifluoroethyl ptoluenesulfonate prepared by reacting 2,2,2-trifluoroethanol with p Flurothyl toluenesulfonyl chloride were placed in another reactor and heated to about 160° to 185°C. The solution of sodium 2,2,2-trifluoroethylate in dioxane was added very slowly over a period of about 1? hours. Bis(2,2,2-trifluoroethyl) ether formed continuously and distilled from the reactor with the dioxane into a cooled receiving vessel. The condensed effluent from the reactor was fractionally distilled, yielding 46.5 parts of products boiling at 55° to 73°C.The crude product was washed successively with concentrated HCl, 62% H2SO4,concentrated H2SO4 and 5% NaOH solution. It was dehydrated over a drying agent and then refractionated in a still. 20 parts of bis(2,2,2trifluoroethyl) ether were recovered (BP 62.5° to 63.5°C).

    Therapeutic Function

    Central stimulant, Convulsant

    Brand name

    Indoklon (Ohmeda).

    InChI:InChI=1/C4H4F6O/c5-3(6,7)1-11-2-4(8,9)10/h1-2H2

    333-36-8 Relevant articles

    Synthesis of trifluoroethyl ethers from 2,2,2-trifluoroethyl chloride (HCFC-133a) in high temperature aqueous medium

    Wu, Kai,Chen, Qing-Yun

    , p. 79 - 83 (2002)

    Treatment of 2,2,2-trifluoroethyl chlori...

    Breaking the Trend: Insight into Unforeseen Reactivity of Alkynes in Cobalt-Catalyzed Weak Chelation-Assisted Regioselective C(4)-H Functionalization of 3-Pivaloyl Indole

    Adhikari, Gopal Krushna Das,Banjare, Shyam Kumar,Dutta, Juhi,Nanda, Tanmayee,Pati, Bedadyuti Vedvyas,Ravikumar, Ponneri C.

    , p. 11579 - 11587 (2021/09/22)

    Unique reactivity of diphenylacetylene h...

    Synthesis method and application of bis(2, 2, 2-trifluoroethyl) ether

    -

    Paragraph 0048-0056, (2021/02/10)

    The invention provides a synthesis metho...

    Synthesis of Fluorinated Dialkyl Carbonates from Carbon Dioxide as a Carbonyl Source

    Sugiyama, Masafumi,Akiyama, Midori,Nishiyama, Kohei,Okazoe, Takashi,Nozaki, Kyoko

    , p. 1775 - 1784 (2020/03/23)

    Fluorinated dialkyl carbonates (DACs), w...

    A trifluoro ethyl ether synthesis method

    -

    Paragraph 0017-0022, (2019/04/13)

    A trifluoro ethyl ether synthesis method...

    333-36-8 Process route

    2,2,2-trifluoroethanol
    75-89-8

    2,2,2-trifluoroethanol

    1,1,1-trifluoro-2-(2,2,2-trifluoroethoxy)ethane
    333-36-8

    1,1,1-trifluoro-2-(2,2,2-trifluoroethoxy)ethane

    Conditions
    Conditions Yield
    2,2,2-trifluoroethanol; With magnesium sulfate; sodium hydroxide; at 60 ℃; for 5h;
    With thionyl chloride; at -5 - 50 ℃; for 4h; Temperature; Inert atmosphere;
    93.3%
    With 1,4-dioxane; sodium 2,2,2-trifluoroethanolate; p-toluenesulfonyl chloride; at 160 - 185 ℃;
    With silver tetrafluoroborate; at 70 ℃; for 12h;
    1,1,1-trifluoro-2-chloroethane
    75-88-7

    1,1,1-trifluoro-2-chloroethane

    2,2,2-trifluoroethanol
    75-89-8

    2,2,2-trifluoroethanol

    1,1,1-trifluoro-2-(2,2,2-trifluoroethoxy)ethane
    333-36-8

    1,1,1-trifluoro-2-(2,2,2-trifluoroethoxy)ethane

    Conditions
    Conditions Yield
    With potassium hydroxide; In 1,2-dimethoxyethane; at 70 ℃; for 4h; Temperature;
    97.4%

    333-36-8 Upstream products

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      75-89-8

      2,2,2-trifluoroethanol

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      110-99-6

      2,2'-oxybis-acetic acid

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      421-06-7

      2-bromo-1,1,1-trifluoroethane

    • 298-14-6
      298-14-6

      potassium hydrogencarbonate

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      1,1,1,2-Tetrafluoro-2-(2,2,2-trifluoro-ethoxy)-ethane

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      2,2,2-trifluoroethyl trifluoroacetate

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      32042-38-9

      2,2,2-trifluoroethyl formate

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