Brief introduction of (4S,5R)-5-(3,5-Bis(trifluoromethyl)phenyl)-4-methyloxazolidin-2-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 875444-08-9

Synthetic Route of 875444-08-9, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.875444-08-9, Name is (4S,5R)-5-(3,5-Bis(trifluoromethyl)phenyl)-4-methyloxazolidin-2-one, molecular formula is C12H9F6NO2. In a Article£¬once mentioned of 875444-08-9

Synthesis and crystal structure of (4S,5R)-5-[3,5-BIS(trifluoromethyl) phenyl]-4-methyl-1,3-oxazolidin-2-one

The crystal structure of the (4S,5R)-5-[3,5-bis(trifluoromethyl)phenyl]-4- methyl-1,3-oxazolidin-2-one has been determined by single crystal X-ray diffraction method. The compound crystallizes in the monoclinic system, space group P2(1) with a = 11.867(4) A, b = 5.6968(19) A, c = 20.258(7) A, alpha = 90.00, beta = 91.866(4), gamma = 90.00, Z = 4, V = 1368.8(8) A3, Dx = 1.520 Mg/m3, F (000) = 632, mu(MoKalpha) = 0.157 mm-1, R = 0.0562 and wR = 0.1744 for 3675 reflections with I > 2sigma(I). X-Ray analysis reveals that the benzene and oxazolidin rings are non-coplanar. The oxazolidin ring displays a twist conformation. The two molecules interact with each other by two strong N-H¡¤¡¤¡¤O hydrogen bonds. Herein, we report the synthesis and crystal structure of (4S,5R)-5-[3,5- bis(trifluoromethyl)phenyl]-4-methyl-1,3-oxazolidin-2-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 875444-08-9

Reference£º
Oxazolidine – Wikipedia,
Oxazolidine | C3H2781NO – PubChem