(Z)-5-(1,2-diphenylvinyl)-4-oxo-4H-chromen-7-yl trifluoromethanesulfonate

Base Information

Chemical Name:(Z)-5-(1,2-diphenylvinyl)-4-oxo-4H-chromen-7-yl trifluoromethanesulfonate
CAS No.:1619229-10-5
Molecular Formula:C₂₄H₁₅F₃O₅S
Molecular Weight:472.441
Hs Code.:

Synonyms:(Z)-5-(1,2-diphenylvinyl)-4-oxo-4H-chromen-7-yl trifluoromethanesulfonate

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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 (Z)-5-(1,2-diphenylvinyl)-4-oxo-4H-chromen-7-yl trifluoromethanesulfonate

Chemical Property:

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Technology Process of (Z)-5-(1,2-diphenylvinyl)-4-oxo-4H-chromen-7-yl trifluoromethanesulfonate

There total 2 articles about (Z)-5-(1,2-diphenylvinyl)-4-oxo-4H-chromen-7-yl trifluoromethanesulfonate 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: 87.0%

: 151895-74-8
7-[(Trifluoromethylsulfonyl)oxy]-benzopyran-4-one

: 501-65-5
diphenyl acetylene

: 1619229-10-5
(Z)-5-(1,2-diphenylvinyl)-4-oxo-4H-chromen-7-yl trifluoromethanesulfonate

Guidance literature:: With silver hexafluoroantimonate; [ruthenium(II)(η⁶-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]₂; copper diacetate; acetic acid; In 1,2-dichloro-ethane; at 100 ℃; stereoselective reaction;
DOI:10.1039/c4cc03602f

Reference yield:

: 151895-74-8
7-[(Trifluoromethylsulfonyl)oxy]-benzopyran-4-one

: 501-65-5
diphenyl acetylene

: 1619229-09-2
(E)-5-(1,2-diphenylvinyl)-4-oxo-4H-chromen-7-yl trifluoromethanesulfonate

: 1619229-10-5
(Z)-5-(1,2-diphenylvinyl)-4-oxo-4H-chromen-7-yl trifluoromethanesulfonate

Guidance literature:: With silver hexafluoroantimonate; [ruthenium(II)(η⁶-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]₂; copper diacetate; acetic acid; In 1,2-dichloro-ethane; at 100 ℃; Overall yield = 79 %; Overall yield = 74.5 mg; stereoselective reaction;
DOI:10.1039/c4cc03602f