Benzoic acid 6-[6-(3-hydroxy-3-methyl-butyl)-7-methoxy-4-oxo-4H-chromen-3-yl]-benzo[1,3]dioxol-5-yl ester

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Chemical Name:Benzoic acid 6-[6-(3-hydroxy-3-methyl-butyl)-7-methoxy-4-oxo-4H-chromen-3-yl]-benzo[1,3]dioxol-5-yl ester
CAS No.:210166-41-9
Molecular Formula:C₂₉H₂₆O₈
Molecular Weight:502.521
Hs Code.:

Synonyms:Benzoic acid 6-[6-(3-hydroxy-3-methyl-butyl)-7-methoxy-4-oxo-4H-chromen-3-yl]-benzo[1,3]dioxol-5-yl ester

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Chemical Property of Benzoic acid 6-[6-(3-hydroxy-3-methyl-butyl)-7-methoxy-4-oxo-4H-chromen-3-yl]-benzo[1,3]dioxol-5-yl ester

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Technology Process of Benzoic acid 6-[6-(3-hydroxy-3-methyl-butyl)-7-methoxy-4-oxo-4H-chromen-3-yl]-benzo[1,3]dioxol-5-yl ester

There total 9 articles about Benzoic acid 6-[6-(3-hydroxy-3-methyl-butyl)-7-methoxy-4-oxo-4H-chromen-3-yl]-benzo[1,3]dioxol-5-yl 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: 85.0%

: 98-88-4
benzoyl chloride

: 210166-23-7
3-(6-Hydroxy-benzo[1,3]dioxol-5-yl)-6-(3-hydroxy-3-methyl-butyl)-7-methoxy-chromen-4-one

: 210166-41-9
Benzoic acid 6-[6-(3-hydroxy-3-methyl-butyl)-7-methoxy-4-oxo-4H-chromen-3-yl]-benzo[1,3]dioxol-5-yl ester

Guidance literature:: With potassium carbonate; In acetone; for 1h; Heating;

Reference yield:

: 3153-75-1
1-(5-iodo-2,4-dimethoxyphenyl)ethan-1-one

: 210166-41-9
Benzoic acid 6-[6-(3-hydroxy-3-methyl-butyl)-7-methoxy-4-oxo-4H-chromen-3-yl]-benzo[1,3]dioxol-5-yl ester

Guidance literature:: Multi-step reaction with 8 steps

1: 92 percent / aluminum bromide / acetonitrile / 0.5 h / Ambient temperature

2: 92 percent / N,N-diisopropylethylamine / CH₂Cl₂ / 0.33 h / Ambient temperature

3: 93 percent / KOH / ethanol / 2 h / 50 °C

4: thallium (III) nitrate trihydrate / CHCl₃ / 2 h / 40 °C

5: 10percent aq. HCl / methanol / 2 h / 75 °C

6: 86 percent / Et₃N, PdCl₂, PPh₃, CuI / dimethylformamide / 0.5 h / 80 °C

7: 70 percent / H₂ / Raney Ni / methanol / 18 °C

8: 85 percent / K₂CO₃ / acetone / 1 h / Heating

With hydrogenchloride; potassium hydroxide; copper(l) iodide; aluminum tri-bromide; hydrogen; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; thallium(III) nitrate; palladium dichloride; nickel; In methanol; ethanol; dichloromethane; chloroform; N,N-dimethyl-formamide; acetone; acetonitrile;

Reference yield:

: 103440-58-0
1-(2-hydroxy-5-iodo-4-methoxyphenyl)ethanone

: 210166-41-9
Benzoic acid 6-[6-(3-hydroxy-3-methyl-butyl)-7-methoxy-4-oxo-4H-chromen-3-yl]-benzo[1,3]dioxol-5-yl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 92 percent / N,N-diisopropylethylamine / CH₂Cl₂ / 0.33 h / Ambient temperature

2: 93 percent / KOH / ethanol / 2 h / 50 °C

3: thallium (III) nitrate trihydrate / CHCl₃ / 2 h / 40 °C

4: 10percent aq. HCl / methanol / 2 h / 75 °C

5: 86 percent / Et₃N, PdCl₂, PPh₃, CuI / dimethylformamide / 0.5 h / 80 °C

6: 70 percent / H₂ / Raney Ni / methanol / 18 °C

7: 85 percent / K₂CO₃ / acetone / 1 h / Heating

With hydrogenchloride; potassium hydroxide; copper(l) iodide; hydrogen; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; thallium(III) nitrate; palladium dichloride; nickel; In methanol; ethanol; dichloromethane; chloroform; N,N-dimethyl-formamide; acetone;