翻訳と辞書
Words near each other
・ Dietrich Hrabak
・ Dietrich I
・ Dietrich I of Isenberg
・ Dietrich I of Metz
・ Dietrich I von Hengebach
・ Dietrich I, Count of Cleves
・ Dietrich II
・ Dietrich II of Isenberg-Limburg
・ Dietrich II, Count of Cleves
・ Dietrich III
・ Dietrich III of Limburg
・ Diethylaluminium cyanide
・ Diethylamine
・ Diethylamino hydroxybenzoyl hexyl benzoate
・ Diethylaminoethyl cellulose
Diethylaminosulfur trifluoride
・ Diethylaniline
・ Diethylcarbamazine
・ Diethylene glycol
・ Diethylene glycol diethyl ether
・ Diethylene glycol dinitrate
・ Diethylenetriamine
・ Diethylethanolamine
・ Diethylhydroxylamine
・ Diethylmercury
・ Diethylpyrocarbonate
・ Diethylstilbestrol
・ Diethylthiambutene
・ Diethyltryptamine
・ Diethylzinc


Dictionary Lists
翻訳と辞書 辞書検索 [ 開発暫定版 ]
スポンサード リンク

Diethylaminosulfur trifluoride : ウィキペディア英語版
Diethylaminosulfur trifluoride

|Section2=
|Section3=
}}
Diethylaminosulfur trifluoride (DAST) is the organosulfur compound with the formula Et2NSF3. This liquid is a fluorinating reagent used for the synthesis of organofluorine compounds. The compound is colourless; older samples assume an orange colour.
==Use in organic synthesis==
DAST converts alcohols to the corresponding alkyl fluorides as well as aldehydes and unhindered ketones to geminal difluorides. Carboxylic acids react no further than the acyl fluoride (sulfur tetrafluoride effects the transformation —CO2H → —CF3). DAST is used in preference to the more classical gaseous SF4, since as a liquid it is more easily handled. Acid-labile substrates are less likely to undergo rearrangement and elimination since DAST is less prone to contamination with acids. Reaction temperatures are milder as well - alcohols typically react at -78 °C and ketones around 0 °C.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
ウィキペディアで「Diethylaminosulfur trifluoride」の詳細全文を読む



スポンサード リンク
翻訳と辞書 : 翻訳のためのインターネットリソース

Copyright(C) kotoba.ne.jp 1997-2016. All Rights Reserved.