Английская Википедия:Isoprenol

Материал из Онлайн справочника
Версия от 08:41, 27 марта 2024; EducationBot (обсуждение | вклад) (Новая страница: «{{Английская Википедия/Панель перехода}} {{chembox | Watchedfields = changed | verifiedrevid = 464369911 | Name = Isoprenol | ImageFile = Structural formula of isoprenol.svg | ImageSize = 200px | ImageName = Structural formula of isoprenol | ImageFile1 = Isoprenol-3D-balls.png | ImageSize1 = 180px | ImageName1 = Ball-and-stick model of prenol | PIN = 3-Methylbut-3-en-1-ol | OtherNames = 3-Methyl-3-buten-1-ol |Section1={{Chemb...»)
(разн.) ← Предыдущая версия | Текущая версия (разн.) | Следующая версия → (разн.)
Перейти к навигацииПерейти к поиску

Шаблон:Chembox

Isoprenol, also known as 3-methylbut-3-en-1-ol, is a hemiterpene alcohol. It is produced industrially as an intermediate to 3-methylbut-2-en-1-ol (prenol): global production in 2001 can be estimated as 6–13 thousand tons.[1]

Isoprenol is produced by the reaction between isobutene (2-methylpropene) and formaldehyde.

The reaction of isobutene with formaldehyde to give isoprenol, the first step in the industrial manufacture of prenol.
The reaction of isobutene with formaldehyde to give isoprenol, the first step in the industrial manufacture of prenol.

The thermodynamically preferred prenol with the more substituted double bond cannot be directly formed in the above reaction, but is produced via a subsequent isomerisation:

The isomerization of isoprenol to prenol, the second step in the industrial manufacture of prenol.
The isomerization of isoprenol to prenol, the second step in the industrial manufacture of prenol.

This isomerisation reaction is catalyzed by any species which can form an allyl complex without excessive hydrogenation of the substrate, for example poisoned palladium catalysts.[2]

Notes

Шаблон:Reflist

References

Шаблон:Reflist

  1. Шаблон:SIDS-ref. Major produce in a world is BASF(Germany) and Kuraray(Japan).
  2. See, e.g., Шаблон:Citation.