2-(3,5-Di-tert-butylbenzylidene)-7-(9-acridinyl)-1-oxo-1,2,3,4-tetrahydronaphthalene

Base Information

Chemical Name:2-(3,5-Di-tert-butylbenzylidene)-7-(9-acridinyl)-1-oxo-1,2,3,4-tetrahydronaphthalene
CAS No.:118656-13-6
Molecular Formula:C₃₈H₃₇NO
Molecular Weight:523.718
Hs Code.:

Synonyms:2-(3,5-Di-tert-butylbenzylidene)-7-(9-acridinyl)-1-oxo-1,2,3,4-tetrahydronaphthalene

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Chemical Property of 2-(3,5-Di-tert-butylbenzylidene)-7-(9-acridinyl)-1-oxo-1,2,3,4-tetrahydronaphthalene

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Technology Process of 2-(3,5-Di-tert-butylbenzylidene)-7-(9-acridinyl)-1-oxo-1,2,3,4-tetrahydronaphthalene

There total 4 articles about 2-(3,5-Di-tert-butylbenzylidene)-7-(9-acridinyl)-1-oxo-1,2,3,4-tetrahydronaphthalene 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: 66.0%

: 17610-00-3
3,5-Di-tert-butylbenzaldehyde

: 111773-14-9
7-(9-Acridinyl)-1-oxo-1,2,3,4-tetrahydronaphthalene

: 118656-13-6
2-(3,5-Di-tert-butylbenzylidene)-7-(9-acridinyl)-1-oxo-1,2,3,4-tetrahydronaphthalene

Guidance literature:: With potassium hydroxide; In methanol; at 70 ℃; for 20h;
DOI:10.1021/ja00186a035

Reference yield:

: 32281-97-3
7-bromo-3,4-dihydro-2H-naphthalen-1-one

: 118656-13-6
2-(3,5-Di-tert-butylbenzylidene)-7-(9-acridinyl)-1-oxo-1,2,3,4-tetrahydronaphthalene

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / p-toluenesulfonic acid / toluene / 12 h / Heating

3: 66 percent / 4percent KOH / methanol / 20 h / 70 °C

With potassium hydroxide; toluene-4-sulfonic acid; In methanol; toluene;
DOI:10.1021/ja00186a035

Reference yield:

: 111773-13-8
7-Bromo-1,2,3,4-tetrahydronaphthalene-1-spiro-2'-(1',3'-dioxacyclopentane)

: 118656-13-6
2-(3,5-Di-tert-butylbenzylidene)-7-(9-acridinyl)-1-oxo-1,2,3,4-tetrahydronaphthalene

Guidance literature:: Multi-step reaction with 2 steps

2: 66 percent / 4percent KOH / methanol / 20 h / 70 °C

With potassium hydroxide; In methanol;
DOI:10.1021/ja00186a035