Английская Википедия:Furoin

Материал из Онлайн справочника
Версия от 16:38, 10 марта 2024; EducationBot (обсуждение | вклад) (Новая страница: «{{Английская Википедия/Панель перехода}} {{Chembox |verifiedrevid = 461114840 |ImageFile = Furoin.png |ImageSize = 100px |IUPACName = 1,2-bis(2-furyl)-2-hydroxy-ethanone |Section1={{Chembox Identifiers |CASNo = 552-86-3 | CASNo_Ref = {{cascite|correct|CAS}} | UNII_Ref = {{fdacite|correct|FDA}} | UNII = FP41RNB020 |ChEMBL_Ref = {{ebicite|correct|EBI}} |ChEMBL = 364893 |EINECS = 209-024-8 |PubChem = 11100 |ChemSpiderID_Ref = {...»)
(разн.) ← Предыдущая версия | Текущая версия (разн.) | Следующая версия → (разн.)
Перейти к навигацииПерейти к поиску

Шаблон:Chembox

Furoin or 1,2-di(furan-2-yl)-2-hydroxyethanone is an organic compound with formula C10H8O4. It can be produced from furfural by a benzoin condensation reaction catalyzed by cyanide ions.[1]

Reactions

Furoin synthesis from furfural is also catalyzed by vitamin B1 (thiamine). In 1957, Ronald Breslow proposed that this reaction involves a relatively stable carbene form of thiamine.[2][3] In the catalytic cycle shown below two molecules of furfural react to give furoin, via a thiazol-2-ylidene catalyst, resulting from loss of one proton at carbon 2 of the thiazolium cation of vitamin B1:

Файл:Breslow1.png
Furoin formation from furfural, catalysed by thiamine

This was the first evidence for the existence of persistent carbenes.

Uses

Furoin has been used as a plasticizer.[1]

References

Шаблон:Reflist