翻訳と辞書
Words near each other
・ 2-Ethyl-1-butanol
・ 2-Ethyl-4,5-dimethylphenol
・ 2-Ethylanthraquinone
・ 2-Ethylhexanoic acid
・ 2-Ethylhexanol
・ 2-Ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine
・ 2-ethylmalate synthase
・ 2-EXPTIME
・ 2-factor theorem
・ 2-Fluoroamphetamine
・ 2-Fluoroethanol
・ 2-Fluoromethamphetamine
・ 2-Formylbenzoate dehydrogenase
・ 2-Formylpyridine
・ 2-functor
2-Furanone
・ 2-furoate—CoA ligase
・ 2-Furoic acid
・ 2-Furonitrile
・ 2-Furoyl chloride
・ 2-furoyl-CoA dehydrogenase
・ 2-graph
・ 2-group
・ 2-haloacid dehalogenase (configuration-inverting)
・ 2-haloacid dehalogenase (configuration-retaining)
・ 2-haloalkanoic acid dehalogenase
・ 2-Headed Shark Attack
・ 2-Heptanol
・ 2-Heptanone
・ 2-hexadecenal reductase


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

2-Furanone : ウィキペディア英語版
2-Furanone

| Section2 =
| Section7 =
}}
2-Furanone, also known as γ-crotonolactone (GCL), is a heterocyclic organic compound. Classified as a lactone, this colourless liquid is colloquially called "butenolide." As a class of compounds, substituted derivatives, which are not in fact prepared from the parent 2-furanone, are called butenolides.
==Synthesis and reactions==
2-Furanone is prepared by oxidation of furfural:
:400px
It exists in equilibrium with the tautomer 2-hydroxyfuran, which serves as an intermediate in the interconversion between the β- and α-furanones. The β form is the more stable. The interconversion is catalyzed by base.
2-Furanones can be converted to furans by a two-step process of reduction followed by dehydration. First the carbon-oxygen double bond is reduced by trimethylsilylation of the oxygen centre.

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「2-Furanone」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.