(3-methoxy-phenyl)-[2-(4-methoxy-phenyl)-1,3-dioxo-indan-2-yl]-acetic acid methyl ester

Base Information

Chemical Name:(3-methoxy-phenyl)-[2-(4-methoxy-phenyl)-1,3-dioxo-indan-2-yl]-acetic acid methyl ester
CAS No.:551929-17-0
Molecular Formula:C₂₆H₂₂O₆
Molecular Weight:430.457
Hs Code.:

Synonyms:(3-methoxy-phenyl)-[2-(4-methoxy-phenyl)-1,3-dioxo-indan-2-yl]-acetic acid methyl ester

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Chemical Property of (3-methoxy-phenyl)-[2-(4-methoxy-phenyl)-1,3-dioxo-indan-2-yl]-acetic acid methyl ester

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Technology Process of (3-methoxy-phenyl)-[2-(4-methoxy-phenyl)-1,3-dioxo-indan-2-yl]-acetic acid methyl ester

There total 1 articles about (3-methoxy-phenyl)-[2-(4-methoxy-phenyl)-1,3-dioxo-indan-2-yl]-acetic acid methyl ester 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: 88.0%

: 117-37-3
anisindione

: 86215-57-8
bromo-(3-methoxy-phenyl)-acetic acid methyl ester

: 551929-17-0
(3-methoxy-phenyl)-[2-(4-methoxy-phenyl)-1,3-dioxo-indan-2-yl]-acetic acid methyl ester

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 50 ℃; for 0.333333h;
DOI:10.1016/S0960-894X(02)00985-X

Reference yield: 72.0%

: 551929-17-0
(3-methoxy-phenyl)-[2-(4-methoxy-phenyl)-1,3-dioxo-indan-2-yl]-acetic acid methyl ester

: 475631-86-8
(3-methoxy-phenyl)-[2-(4-methoxy-phenyl)-indan-2-yl]-acetic acid

Guidance literature:: With hydrogen; acetic acid; palladium dihydroxide; In ethanol; ethyl acetate; for 39h;
DOI:10.1016/S0960-894X(02)00985-X

Reference yield:

: 551929-17-0
(3-methoxy-phenyl)-[2-(4-methoxy-phenyl)-1,3-dioxo-indan-2-yl]-acetic acid methyl ester

: 551929-19-2
C₂₅H₂₂O₂

Guidance literature:: Multi-step reaction with 5 steps

1: 72 percent / H₂; AcOH / Pd(OH)2/C / ethyl acetate; ethanol / 39 h

2: PCl₅ / CH₂Cl₂ / 1 h / 0 °C

3: AlCl₃ / CH₂Cl₂ / 1.5 h / 0 °C

4: NaBH₄ / methanol; tetrahydrofuran / 2 h

5: TsOH / benzene / 2 h / Heating

With sodium tetrahydroborate; aluminium trichloride; phosphorus pentachloride; hydrogen; toluene-4-sulfonic acid; acetic acid; palladium dihydroxide; In tetrahydrofuran; methanol; ethanol; dichloromethane; ethyl acetate; benzene; 3: Friedel-Crafts cyclization;
DOI:10.1016/S0960-894X(02)00985-X