[ジフルオロ(フェニルスルファニル)メチル]トリメチルシラン

[ジフルオロ(フェニルスルファニル)メチル]トリメチルシラン 化学構造式
536975-49-2
CAS番号.
536975-49-2
化学名:
[ジフルオロ(フェニルスルファニル)メチル]トリメチルシラン
别名:
[ジフルオロ(フェニルスルファニル)メチル]トリメチルシラン
英語名:
[[difluoro(triMethylsilyl)Methyl]thio]-Benzene
英語别名:
[Difluoro(phenylthio)Methyl]triMethylsilane;[[difluoro(triMethylsilyl)Methyl]thio]-Benzene;[Difluoro(phenylsulfanyl)methyl]trimethylsilane;Benzene, [[difluoro(trimethylsilyl)methyl]thio]-
CBNumber:
CB52644988
化学式:
C10H14F2SSi
分子量:
232.37
MOL File:
536975-49-2.mol

[ジフルオロ(フェニルスルファニル)メチル]トリメチルシラン 物理性質

溶解性:
ヘキサン、テトラヒドロフラン (THF)、CH2Cl2、ジメチルホルムアミド (DMF) などのほとんどの有機溶媒に可溶。

安全性情報

HSコード  29309090

[ジフルオロ(フェニルスルファニル)メチル]トリメチルシラン 価格 もっと(2)

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入
富士フイルム和光純薬株式会社(wako) W01MAS125432 [ジフルオロ(フェニルスルファニル)メチル]トリメチルシラン
[Difluoro(phenylsulfanyl)methyl]trimethylsilane
536975-49-2 1g ¥407100 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) W01MAS125432 [ジフルオロ(フェニルスルファニル)メチル]トリメチルシラン
[Difluoro(phenylsulfanyl)methyl]trimethylsilane
536975-49-2 5g ¥1062600 2024-03-01 購入

[ジフルオロ(フェニルスルファニル)メチル]トリメチルシラン 化学特性,用途語,生産方法

説明

An effective reagent to introduce difluoromethyl groups into carbonyls, imines, enamines, and alkyl halides. Not only various simple aldehydes and ketones, but also functionalized carbonyls such as α- and γ-ketoesters and cyclic imides can be difluoro(phenylthio)methylated in high yields under the activation of a catalytic amount of Lewis bases. The substitution reaction proceeds well with primary alkyl bromides and iodides as the limiting reactant when cesium fluorode/15-crown-5 is used as the fluoride source/additive. Under radical conditions, the difluoro(phenylthio)methyl compounds containing vinyl functional groups can form 5- or 6-membered rings via intramolecular cyclization.

物理的性質

colorless liquid; bp 86–87?C/4 mmHg.

使用

Organofluorine compounds have received remarkable interest in recent years due to their wide-ranging biological effects. The development of general synthetic routes to such compounds and the use of new fluorinated compounds as building blocks are of great importance. Of particular interest is the selective incorporation of the gem-difluoromethylene group ‘CF2’ into organic molecules. The report on the synthesis of PhSCF2SiMe3 was published in 2003 by Prakash et al., and the reagent has become one of the most versatile and efficient nucleophilic (phenylthio)difluoromethylating reagents.
When excess potassium t-butoxide was used as a promoter, PhSCF2SiMe3 reacted with diphenyl disulfide to give the corresponding dithioacetal in 85% yield (eq 8).

製造方法

[difluoro(phenylthio)methyl]trimethylsilane (PhSCF2SiMe3) was prepared for the first time by Prakash et al.,1 using the Barbier coupling reaction of bromodifluoromethylphenyl sulfide,2 prepared from dibromodifluoromethane and sodium benzenethiolate,3 magnesium metal, and chlorotrimethylsilane (TMSCl) in DMF (eq 1).

説明図

反応性

(1) Difluoromethylation of aldehydes and ketones.
説明図
(2) Difluoromethylation of imines and enamines.
説明図
(3) (Phenylthio)difluoromethylation of imines for further cyclizations.
説明図
(4) Difluoromethylation of alkyl halides.
説明図

[ジフルオロ(フェニルスルファニル)メチル]トリメチルシラン 上流と下流の製品情報

原材料

準備製品


[ジフルオロ(フェニルスルファニル)メチル]トリメチルシラン 生産企業

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  • 536975-49-2
  • [[difluoro(triMethylsilyl)Methyl]thio]-Benzene
  • [Difluoro(phenylthio)Methyl]triMethylsilane
  • [Difluoro(phenylsulfanyl)methyl]trimethylsilane
  • Benzene, [[difluoro(trimethylsilyl)methyl]thio]-
  • [ジフルオロ(フェニルスルファニル)メチル]トリメチルシラン
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