1,8,9-Triphenylanthracen

Base Information

Chemical Name:1,8,9-Triphenylanthracen
CAS No.:33522-39-3
Molecular Formula:C₃₂H₂₂
Molecular Weight:406.527
Hs Code.:

Synonyms:

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Chemical Property of 1,8,9-Triphenylanthracen

Chemical Property:

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Technology Process of 1,8,9-Triphenylanthracen

There total 12 articles about 1,8,9-Triphenylanthracen 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:

: 16939-57-4
(E)-buta-1,3-dienylbenzene

: 33522-39-3
1,8,9-Triphenylanthracen

Guidance literature:: Multi-step reaction with 6 steps

1: CCl₃CO₂H / benzene

2: Na₂Cr₂O₇, aq. H₂SO₄ / acetic acid

3: benzene

4: KOH, O₂ / ethanol

5: Sn, aq. HCl / acetic acid

6: (i), (ii) aq. HCl

With hydrogenchloride; potassium hydroxide; tin; sodium dichromate; sulfuric acid; oxygen; trichloroacetic acid; In ethanol; acetic acid; benzene;
DOI:10.1021/jo00972a017

Reference yield:

: 33522-29-1
5-phenyl-1,4-naphthoquinone

: 33522-39-3
1,8,9-Triphenylanthracen

Guidance literature:: Multi-step reaction with 4 steps

1: benzene

2: KOH, O₂ / ethanol

3: Sn, aq. HCl / acetic acid

4: (i), (ii) aq. HCl

With hydrogenchloride; potassium hydroxide; tin; oxygen; In ethanol; acetic acid; benzene;
DOI:10.1021/jo00972a017

Reference yield:

: 82-43-9
1,8-dichloroanthraquinone

: 33522-39-3
1,8,9-Triphenylanthracen

Guidance literature:: Multi-step reaction with 6 steps

1: KOAc, Cu(OAc)2 / nitrobenzene

2: aq. H₂SO₄

3: (i) NaNO₂, aq. H₂SO₄, (ii) aq. KI

4: (i) CuBr, (ii) O₂

5: Sn, aq. HCl / acetic acid

6: (i), (ii) aq. HCl

With hydrogenchloride; tin; copper diacetate; sulfuric acid; potassium acetate; In acetic acid; nitrobenzene;
DOI:10.1021/jo00972a017