1,3-dihydroxy-4-(3,3-dimethylallyl)-5-benzyloxyacridone

Base Information

Chemical Name:1,3-dihydroxy-4-(3,3-dimethylallyl)-5-benzyloxyacridone
CAS No.:108937-61-7
Molecular Formula:C₂₅H₂₃NO₄
Molecular Weight:401.462
Hs Code.:

Synonyms:

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Chemical Property of 1,3-dihydroxy-4-(3,3-dimethylallyl)-5-benzyloxyacridone

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Technology Process of 1,3-dihydroxy-4-(3,3-dimethylallyl)-5-benzyloxyacridone

There total 5 articles about 1,3-dihydroxy-4-(3,3-dimethylallyl)-5-benzyloxyacridone 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:

: 63110-81-6
1,3-dihydroxy-5-methoxy-9(10H)-acridinone

: 108937-61-7
1,3-dihydroxy-4-(3,3-dimethylallyl)-5-benzyloxyacridone

Guidance literature:: Multi-step reaction with 4 steps

1: 900 mg / methanol; diethyl ether / 12 h / 0 °C

2: 10 mg / conc. H₂SO₄ / 12 h

3: 4 g / NaHCO₃, NaI / acetone / 18 h / Heating

4: 300 mg / BF₃ etherate / dioxane / 2 h

With sulfuric acid; boron trifluoride diethyl etherate; sodium hydrogencarbonate; sodium iodide; In 1,4-dioxane; methanol; diethyl ether; acetone;

Reference yield:

: 85990-00-7
1,3,5-trihydroxy-9(10H)-acridinone

: 108937-61-7
1,3-dihydroxy-4-(3,3-dimethylallyl)-5-benzyloxyacridone

Guidance literature:: Multi-step reaction with 2 steps

1: 4 g / NaHCO₃, NaI / acetone / 18 h / Heating

2: 300 mg / BF₃ etherate / dioxane / 2 h

With boron trifluoride diethyl etherate; sodium hydrogencarbonate; sodium iodide; In 1,4-dioxane; acetone;

Reference yield:

: 85990-01-8
1-hydroxy-3,5-dimethoxy-9(10H)-acridinone

: 108937-61-7
1,3-dihydroxy-4-(3,3-dimethylallyl)-5-benzyloxyacridone

Guidance literature:: Multi-step reaction with 3 steps

1: 10 mg / conc. H₂SO₄ / 12 h

2: 4 g / NaHCO₃, NaI / acetone / 18 h / Heating

3: 300 mg / BF₃ etherate / dioxane / 2 h

With sulfuric acid; boron trifluoride diethyl etherate; sodium hydrogencarbonate; sodium iodide; In 1,4-dioxane; acetone;