9-[1-(2-methoxy-4-methoxycarbonylmethoxyphenyl)]-6-hydroxy-3H-xanthen-3-one

Base Information

Chemical Name:9-[1-(2-methoxy-4-methoxycarbonylmethoxyphenyl)]-6-hydroxy-3H-xanthen-3-one
CAS No.:936030-65-8
Molecular Formula:C₂₃H₁₈O₇
Molecular Weight:406.392
Hs Code.:

Synonyms:9-[1-(2-methoxy-4-methoxycarbonylmethoxyphenyl)]-6-hydroxy-3H-xanthen-3-one

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Chemical Property of 9-[1-(2-methoxy-4-methoxycarbonylmethoxyphenyl)]-6-hydroxy-3H-xanthen-3-one

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Technology Process of 9-[1-(2-methoxy-4-methoxycarbonylmethoxyphenyl)]-6-hydroxy-3H-xanthen-3-one

There total 6 articles about 9-[1-(2-methoxy-4-methoxycarbonylmethoxyphenyl)]-6-hydroxy-3H-xanthen-3-one 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: 63.0%

: 936030-64-7
9-[1-(4-hydroxy-2-methoxyphenyl)]-6-hydroxy-3H-xanthen-3-one

: 96-32-2
bromoacetic acid methyl ester

: 936030-65-8
9-[1-(2-methoxy-4-methoxycarbonylmethoxyphenyl)]-6-hydroxy-3H-xanthen-3-one

Guidance literature:: With caesium carbonate; In N,N-dimethyl-formamide; at 25 ℃;
DOI:10.1021/ja067710a

Reference yield:

: 936030-63-6
9-{1-[4-(tert-butyldimethylsilyloxy)-2-methoxyphenyl]}-6-hydroxy-3H-xanthen-3-one

: 936030-65-8
9-[1-(2-methoxy-4-methoxycarbonylmethoxyphenyl)]-6-hydroxy-3H-xanthen-3-one

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / aq. HCl / 5 h / Heating

2: 63 percent / Cs₂CO₃ / dimethylformamide / 25 °C

With hydrogenchloride; caesium carbonate; In N,N-dimethyl-formamide;
DOI:10.1021/ja067710a

Reference yield:

: 6626-15-9
4-Bromoresorcinol

: 936030-65-8
9-[1-(2-methoxy-4-methoxycarbonylmethoxyphenyl)]-6-hydroxy-3H-xanthen-3-one

Guidance literature:: Multi-step reaction with 6 steps

1.1: K₂CO₃ / acetone / Heating

1.2: 100 percent / acetone / Heating

2.1: 89 percent / aq. NaOH / methanol / 1.5 h / Heating

3.1: 76.7 percent / imidazole / dimethylformamide / 25 °C

4.1: tert-butyllithium / tetrahydrofuran; pentane / -78 °C

4.2: tetrahydrofuran; pentane / 0.5 h / -78 °C

4.3: 3.7 percent / aq. HCl / tetrahydrofuran; pentane

5.1: 70 percent / aq. HCl / 5 h / Heating

6.1: 63 percent / Cs₂CO₃ / dimethylformamide / 25 °C

With 1H-imidazole; hydrogenchloride; sodium hydroxide; tert.-butyl lithium; potassium carbonate; caesium carbonate; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; acetone; pentane;
DOI:10.1021/ja067710a