Английская Википедия:2-Furanone

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Версия от 13:49, 21 декабря 2023; EducationBot (обсуждение | вклад) (Новая страница: «{{Английская Википедия/Панель перехода}} {{chembox | Watchedfields = changed | verifiedrevid = 477213431 | ImageFileL1 = Furan-2-one.svg | ImageSizeL1 = 120 | ImageAltL1 = Skeletal formula of 2-furanone | ImageFileR1 = 2-Furanone-3D-balls.png | ImageSizeR1 = 130 | ImageAltR1 = Ball-and-stick model of the 2-furanone molecule | PIN = Furan-2(5''H'')-one | OtherNames = Furan-2-one, γ-crotonolactone, butenolide, 5''H''-furan-2-o...»)
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Шаблон:Chembox

2-Furanone is a heterocyclic organic compound. It is also known as γ-crotonolactone (GCL), as it is formally the lactone derived from γ-hydroxyisocrotonic acid. The chemical is colloquially called "butenolide", and is the parent structure for the butenolide class of compounds. It is a colourless liquid.

Synthesis and reactions

2-Furanone is prepared by oxidation of furfural:[1]

Файл:Synthesis 2-Furanone.svg

It exists in equilibrium with the tautomer 2-hydroxyfuran, which serves as an intermediate in the interconversion between the β- and α-furanones.Шаблон:Explain 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.

See also

References

Шаблон:Reflist


Шаблон:GHBergics