More research is needed about (Tetrahydrofuran-3-yl)methanamine

We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 165253-31-6, and how the biochemistry of the body works.Application of 165253-31-6

Application of 165253-31-6, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.165253-31-6, Name is (Tetrahydrofuran-3-yl)methanamine, molecular formula is C5H11NO. In a Patent,once mentioned of 165253-31-6

The invention relates to a kind of dinotefuran synthesis method, the method is to dihydro benzofuran as raw materials, through Vilsmeier – Haack reaction to obtain the dihydrofuran – 3 – formaldehyde, then under the effects of catalyst reduction amination to obtain 3 – aminomethyl tetrahydrofuran, finally with the 1, 3 – dimethyl – 2 – nitro-isourea condensation to obtain the compound dinotefuran. The method of the Vilsmeier – Haack reaction applied to the creativity of the dinotefuran synthesis, using the generated aldehyde intermediate, so that the aldehyde reduction amination with double bond reduction at the same time, reducing reaction steps, reducing the complexity of the operation, and the synthesis of intermediates line is greatly shortened, the process cost is reduced, in addition from the selection of the raw materials on the 2, 3 – dihydrofuran and 2, 5 – dihydro benzofuran can be used for aldehyde synthesis, more broad selection of raw materials, is the process of the practicability is stronger. (by machine translation)

We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 165253-31-6, and how the biochemistry of the body works.Application of 165253-31-6

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