トリフルオロメタンスルホン酸無水物

危険有害性情報のコード(GHS)

• 絵表示(GHS)

  

• 注意喚起語

  Danger

• 危険有害性情報

  H272：火災助長のおそれ；酸化性物質

  H302：飲み込むと有害

  H314：重篤な皮膚の薬傷?眼の損傷

  H335：呼吸器への刺激のおそれ

• 注意書き

  P210：熱/火花/裸火/高温のもののような着火源から遠ざ けること。－禁煙。

  P220：衣類/．．．/可燃物から遠ざけること。

  P280：保護手袋/保護衣/保護眼鏡/保護面を着用するこ と。

  P301+P312：飲み込んだ場合：気分が悪い時は医師に連絡する こと。

  P303+P361+P353：皮膚（または髪）に付着した場合：直ちに汚染された衣 類をすべて脱ぐこと/取り除くこと。皮膚を流水/シャワー で洗うこと。

  P305+P351+P338：眼に入った場合：水で数分間注意深く洗うこと。次にコ ンタクトレンズを着用していて容易に外せる場合は外す こと。その後も洗浄を続けること。

トリフルオロメタンスルホン酸無水物 価格

MSDS Information

• Trifluoromethanesulfonic anhydride

トリフルオロメタンスルホン酸無水物 化学特性,用途語,生産方法

• 外観

  無色～うすい黄色、液体

• 用途

  本製品は主に医農薬中間体などの合成原料（トリフラート化剤）として利用されております。原料からの一環製造、および当社独自のプロセスにより高純度品のご提供が可能です。

• 用途

  有機合成(和光試薬時報Vol.62 No.3,p.29(1994))。

• 説明

  Trifluoromethanesulfonic anhydride, also known as triflic anhydride, has proven to be an extraordinary reagent for a broad range of transformations. As a commercially and readily available reagent, It has been widely used in synthetic chemistry due to its high electrophilicity. Given its high affinity towards O-nucleophiles, reaction with alcohols, carbonyls, sulfur phosphorus- and iodine oxides towards the formation of the corresponding triflates is strongly favored. As one of the premier leaving groups in organic chemistry, the generated triflates then open the door to various downstream transformations, including (but not limited to) substitution reactions, cross-coupling processes, redox reactions, and rearrangements[1-2].

• 化学的特性

  clear colorless to light brown liquid

• 使用

  Trifluoromethanesulfonic Anhydride is a strong electrophile used in chemical synthesis for introducing the triflyl group.

• 危険性

  May be corrosive to metals. Harmful if swallowed. Causes severe skin burns and eye damage.

• 合成

  The synthesis of Trifluoromethanesulfonic anhydride is as follows:
  A dry, 100-ml., round-bottomed flask is charged with 36.3 g. (0.242 mole) of trifluoromethanesulfonic acid (Note 1) and 27.3 g. (0.192 mole) of phosphorus pentoxide (Note 2). The flask is stoppered and allowed to stand at room temperature for at least 3 hours. During this period the reaction mixture changes from a slurry to a solid mass. The flask is fitted with a short-path distilling head and heated first with a stream of hot air from a heat gun and then with the flame from a small burner.

  The flask is heated until no more trifluoromethanesulfonic anhydride distills, b.p. 82–115°, yielding 28.4–31.2 g. (83–91%) of the anhydride, a colorless liquid. Although this product is sufficiently pure for use in the next step, the remaining acid may be removed from the anhydride by the following procedure. A slurry of 3.2 g. of phosphorus pentoxide in 31.2 g. of the crude anhydride is stirred at room temperature in a stoppered flask for 18 hours. After the reaction flask has been fitted with a short-path distilling head, it is heated with an oil bath, yielding 0.7 g. of forerun, b.p. 74–81°, followed by 27.9 g. of the pure trifluoromethanesulfonic acid anhydride, b.p. 81–84° .
  

• 貯蔵

  Store in a cool, dry, wellventilated area.  Moisture sensitive.

• 純化方法

  It can be freshly prepared from the anhydrous acid (11.5g) and P2O5 (11.5g, or half this weight) by setting aside at room temperature for 1hour, distilling off volatile products then distil it through a short Vigreux column. It is readily hydrolysed by H2O and decomposes appreciably after a few days to liberate SO2 and produce a viscous liquid. Store it dry at low temperatures. [Burdon et al. J Chem Soc 2574 1957, Beard et al. J Org Chem 38 373 1973, Beilstein 3 IV 35.]

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