翻訳と辞書
Words near each other
・ Sodium aluminium sulfate
・ Sodium aluminosilicate
・ Sodium amalgam
・ Sodium amide
・ Sodium apolate
・ Sodium arsenate
・ Sodium arsenite
・ Sodium ascorbate
・ Sodium aurothiomalate
・ Sodium aurothiosulfate
・ Sodium azide
・ Sodium benzoate
・ Sodium bicarbonate
・ Sodium bicarbonate rocket
・ Sodium bifluoride
Sodium bis(2-methoxyethoxy)aluminumhydride
・ Sodium bis(trimethylsilyl)amide
・ Sodium bismuthate
・ Sodium bisulfate
・ Sodium bisulfite
・ Sodium borohydride
・ Sodium bromate
・ Sodium bromide
・ Sodium butyrate
・ Sodium carbonate
・ Sodium Carbonate Company
・ Sodium cellulose phosphate
・ Sodium channel
・ Sodium channel blocker
・ Sodium channel opener


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

Sodium bis(2-methoxyethoxy)aluminumhydride : ウィキペディア英語版
Sodium bis(2-methoxyethoxy)aluminumhydride

|Section2=
|Section3=
}}
Sodium bis(2-methoxyethoxy)aluminumhydride (trade names Red-Al, Synhydrid, Vitride) is an organoaluminium compound with the formula NaAlH2(OCH2CH2OCH3)2. The trade name Red-Al refers to its being a ''red''ucing ''al''uminium compound. It is a predominantly as a reducing agent in organic synthesis. The compound features a tetrahedral aluminium center attached to two hydride and two alkoxide groups, the latter derived from 2-methoxyethanol. Commercial solutions are colourless/pale yellow and viscous. At low temperatures, the solution solidifies to a glassy pulverizable substance. No sharp melting point was found.
Sodium bis(2-methoxyethoxy)aluminumhydride is a versatile hydride reducing agent. It readily converts aldehydes, ketones, carboxylic acids, esters, acyl halides, and anhydrides to primary alcohols. The cyclic compounds such a lactones and epoxides are reduced to diols. Nitrogen derivates such a amides, nitriles, imines, and most other organonitrogen compounds are reduced to the corresponding amines. Nitroarenes can be converted to azoxyarenes, azoarenes, or hydroazoarenes, depending on the reaction conditions.
Some common functional group reductions using sodium bis(2-methoxyethoxy)aluminumhydride can be found below:
==Comparison with lithium aluminium hydride==
As a reagent, sodium bis(2-methoxyethoxy)aluminumhydride is comparable with lithium aluminum hydride (LAH, LiAlH4).
It is a safer substitute for LAH and related hydrides. Sodium bis(2-methoxyethoxy)aluminumhydride exhibits similar reducing effects, but does not have the inconvenient pyrophoric nature, short shelf-life, or limited solubility of LAH. Upon contact with air and moisture, Sodium bis(2-methoxyethoxy)aluminumhydride reacts exothermically but does not ignite, and tolerates temperatures up to 200 °C. Under dry conditions it has unlimited shelf life. It is soluble in aromatic solvents, whereas LAH is only soluble in ethers. For example, a solution greater than 60 wt.% concentration in toluene is commercially available. The reagent can be modified to effect partial reductions.〔

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「Sodium bis(2-methoxyethoxy)aluminumhydride」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.