10-hydroxy-10-[7-methoxy-3-(2-pivaloyloxymethylphenyl)hept-3-ene-1,5-diynyl]-10H-anthracen-9-one

Base Information

Chemical Name:10-hydroxy-10-[7-methoxy-3-(2-pivaloyloxymethylphenyl)hept-3-ene-1,5-diynyl]-10H-anthracen-9-one
CAS No.:662723-10-6
Molecular Formula:C₃₄H₃₀O₅
Molecular Weight:518.609
Hs Code.:

Synonyms:10-hydroxy-10-[7-methoxy-3-(2-pivaloyloxymethylphenyl)hept-3-ene-1,5-diynyl]-10H-anthracen-9-one

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Chemical Property of 10-hydroxy-10-[7-methoxy-3-(2-pivaloyloxymethylphenyl)hept-3-ene-1,5-diynyl]-10H-anthracen-9-one

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Technology Process of 10-hydroxy-10-[7-methoxy-3-(2-pivaloyloxymethylphenyl)hept-3-ene-1,5-diynyl]-10H-anthracen-9-one

There total 8 articles about 10-hydroxy-10-[7-methoxy-3-(2-pivaloyloxymethylphenyl)hept-3-ene-1,5-diynyl]-10H-anthracen-9-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: 52.0%

: 84-65-1
9,10-phenanthrenequinone

: 662723-09-3
7-methoxy-3-(2-pivaloyloxymethylphenyl)-1,5-heptadiyn-3-(E)-ene

: 662723-10-6
10-hydroxy-10-[7-methoxy-3-(2-pivaloyloxymethylphenyl)hept-3-ene-1,5-diynyl]-10H-anthracen-9-one

Guidance literature:: With ethylmagnesium bromide; In tetrahydrofuran; dichloromethane; Heating;

Reference yield:

: 3282-30-2
pivaloyl chloride

: 662723-10-6
10-hydroxy-10-[7-methoxy-3-(2-pivaloyloxymethylphenyl)hept-3-ene-1,5-diynyl]-10H-anthracen-9-one

Guidance literature:: Multi-step reaction with 7 steps

1: 62 percent / NaH / tetrahydrofuran / 0 - 20 °C

2: tetrabutylammonium bromide; aq. NaClO / ethyl acetate / 0 - 20 °C

3: 44.6 g / tetrahydrofuran / 0.5 h / 0 °C

4: 87 percent / CrO₃; aq. H₂SO₄ / acetone / 0 - 20 °C

5: 73 percent / Zn / tetrahydrofuran / 0.5 h / Heating

6: 81 percent / triethylamine; methanesulfonyl chloride / CH₂Cl₂ / 2 h / 0 °C

7: 52 percent / EtMgBr / tetrahydrofuran; CH₂Cl₂ / Heating

With chromium(VI) oxide; sodium hypochlorite; sulfuric acid; ethylmagnesium bromide; tetrabutylammomium bromide; sodium hydride; methanesulfonyl chloride; triethylamine; zinc; In tetrahydrofuran; dichloromethane; ethyl acetate; acetone;

Reference yield:

: 612-14-6
phthalyl alcohol

: 662723-10-6
10-hydroxy-10-[7-methoxy-3-(2-pivaloyloxymethylphenyl)hept-3-ene-1,5-diynyl]-10H-anthracen-9-one

Guidance literature:: Multi-step reaction with 7 steps

1: 62 percent / NaH / tetrahydrofuran / 0 - 20 °C

2: tetrabutylammonium bromide; aq. NaClO / ethyl acetate / 0 - 20 °C

3: 44.6 g / tetrahydrofuran / 0.5 h / 0 °C

4: 87 percent / CrO₃; aq. H₂SO₄ / acetone / 0 - 20 °C

5: 73 percent / Zn / tetrahydrofuran / 0.5 h / Heating

6: 81 percent / triethylamine; methanesulfonyl chloride / CH₂Cl₂ / 2 h / 0 °C

7: 52 percent / EtMgBr / tetrahydrofuran; CH₂Cl₂ / Heating

With chromium(VI) oxide; sodium hypochlorite; sulfuric acid; ethylmagnesium bromide; tetrabutylammomium bromide; sodium hydride; methanesulfonyl chloride; triethylamine; zinc; In tetrahydrofuran; dichloromethane; ethyl acetate; acetone;