4-methyl-2-morpholino-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)benzamide

Base Information

Chemical Name:4-methyl-2-morpholino-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)benzamide
CAS No.:1465827-33-1
Molecular Formula:C₁₉H₁₅F₇N₂O₂
Molecular Weight:436.329
Hs Code.:

Synonyms:4-methyl-2-morpholino-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)benzamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 4-methyl-2-morpholino-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)benzamide

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Technology Process of 4-methyl-2-morpholino-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)benzamide

There total 2 articles about 4-methyl-2-morpholino-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)benzamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 46.0%

: 110-91-8,99108-56-2
morpholine

: 1402736-42-8
C₁₅H₈F₇NO

: 1465827-33-1
4-methyl-2-morpholino-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)benzamide

Guidance literature:: With 2,4,4-trimethyl oxazoline; lithium acetate; cesium acetate; copper diacetate; copper(I) bromide; In dimethyl sulfoxide; at 100 ℃; for 6h;
DOI:10.1039/C6SC03383K

Reference yield:

: 1402736-42-8
C₁₅H₈F₇NO

: 1452757-48-0
N-benzoyloxylmorpholine

: 1465827-33-1
4-methyl-2-morpholino-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)benzamide

: 1465827-47-7
4-methyl-2,6-di-morpholino-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)benzamide

Guidance literature:: With [ruthenium(II)(η⁶-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]₂; potassium carbonate; In acetone; at 20 ℃; for 36h; Overall yield = 94 %; Schlenk technique;
DOI:10.1021/ol402515s