6,8,15,17-tetraphenyl-6,17:8,15-dioxido-6,6a,7,7a,8,15,15a,16,16a,17-decahydro-7,16-heptacene quinone

Base Information

Chemical Name:6,8,15,17-tetraphenyl-6,17:8,15-dioxido-6,6a,7,7a,8,15,15a,16,16a,17-decahydro-7,16-heptacene quinone
CAS No.:627528-34-1
Molecular Formula:C₅₄H₃₆O₄
Molecular Weight:748.877
Hs Code.:

Synonyms:6,8,15,17-tetraphenyl-6,17:8,15-dioxido-6,6a,7,7a,8,15,15a,16,16a,17-decahydro-7,16-heptacene quinone

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Chemical Property of 6,8,15,17-tetraphenyl-6,17:8,15-dioxido-6,6a,7,7a,8,15,15a,16,16a,17-decahydro-7,16-heptacene quinone

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Technology Process of 6,8,15,17-tetraphenyl-6,17:8,15-dioxido-6,6a,7,7a,8,15,15a,16,16a,17-decahydro-7,16-heptacene quinone

There total 1 articles about 6,8,15,17-tetraphenyl-6,17:8,15-dioxido-6,6a,7,7a,8,15,15a,16,16a,17-decahydro-7,16-heptacene quinone 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: 84.0%

: 18929-57-2
1,3-diphenylnaphtho[2,3-c]furan

: 106-51-4
p-benzoquinone

: 627528-34-1
6,8,15,17-tetraphenyl-6,17:8,15-dioxido-6,6a,7,7a,8,15,15a,16,16a,17-decahydro-7,16-heptacene quinone

Guidance literature:: In benzene; at 20 ℃; for 0.0833333h;
DOI:10.1021/ol0356791

Reference yield: 77.3%

: 627528-34-1
6,8,15,17-tetraphenyl-6,17:8,15-dioxido-6,6a,7,7a,8,15,15a,16,16a,17-decahydro-7,16-heptacene quinone

: 627528-35-2
6,8,15,17-tetraphenylheptacene-7,16-quinone

Guidance literature:: With toluene-4-sulfonic acid; In benzene;
DOI:10.1021/ol0356791

Reference yield:

: 627528-34-1
6,8,15,17-tetraphenyl-6,17:8,15-dioxido-6,6a,7,7a,8,15,15a,16,16a,17-decahydro-7,16-heptacene quinone

: 5,7,9,14,16,18-hexahydro-6,8,15,17-tetraphenylheptacene

Guidance literature:: Multi-step reaction with 2 steps

1: 77 percent / p-tosic acid / benzene

2: 100 percent / HI; AcOH / 72 h

With hydrogen iodide; toluene-4-sulfonic acid; acetic acid; In benzene;
DOI:10.1021/ol0356791