Synthetic Route of 165253-31-6, 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.165253-31-6, Name is (Tetrahydrofuran-3-yl)methanamine, molecular formula is C5H11NO. In a article£¬once mentioned of 165253-31-6
A dinotefuran intermediate 3 – amino methyl tetrahydrofuran preparation method (by machine translation)
The invention relates to a kind of dinotefuran intermediate 3 – amino methyl tetrahydrofuran preparation method, specifically it is to cyano acetic acid ester as the raw material, first with 1, 2 – dihalo ethane condensation reaction to obtain the intermediate 2 – halogenated ethyl – 2 – cyano – acetate, followed by a further reduction to obtain intermediate 2 – halogenated ethyl – 2 – cyano – ethanol, then intermediate 2 – halogenated ethyl – 2 – cyano – ethanol cyclization to obtain intermediate 3 – cyano tetrahydrofuran; the final 3 – cyano tetrahydrofuran obtained by catalytic hydrogenation of dinotefuran intermediate 3 – amino methyl tetrahydrofuran. Preparation method of the invention, raw materials are easy, simple operation, low production cost, and thus is suitable for industrial production. (by machine translation)
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 165253-31-6
Reference£º
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem