Extracurricular laboratory:new discovery of 3-Methyldihydrofuran-2(3H)-one

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 1679-47-6

Reference of 1679-47-6, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.1679-47-6, Name is 3-Methyldihydrofuran-2(3H)-one, molecular formula is C5H8O2. In a article£¬once mentioned of 1679-47-6

Preparation of 2-(3-Bromo-1-methylpropyl)-1,3-dioxolan and the Corresponding Chloride from 2-Methylbutyrolactone

Lithium aluminium hydride reduction of ethyl 4-chloro-2-methylbutanoate (4a), derived from 3-methyldihydrofuran-2(3H)-one (2-methylbutyrolactone) (1), gave 4-chloro-2-methylbutan-1-ol (5a), oxidation of which with pyridinium chlorochromate afforded 4-chloro-2-methylbutanal (8a).The aldehyde (8a) was converted into 2-(3′-chloro-1′-methylpropyl)-1,3-dioxolan (7a) in 47percent overall yield from (1). 2-(3′-Bromo-1′-methylpropyl)-1,3-dioxolan (7b) was similarly obtained in 49percent overall yield from (1).Attempted conversion of 3-methyltetrahydrofuran-2-ol (2) into the corresponding cyclic ethylene acetal gave epimeric mixtures of 2-(3′-methyltetrahydrofuran-2′-yloxy)ethanol (6) and 2,2′-ethylenedioxybis(3-methyltetrahydrofuran) (9).

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 1679-47-6

Reference£º
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem