3-acetyl-3,5,12-trihydroxy-6,11-dioxo-1,2,3,4,6,11-hexahydro-1-naphthacenyl 2-(acetyloxy)-2-phenylethanoate

Base Information

Chemical Name:3-acetyl-3,5,12-trihydroxy-6,11-dioxo-1,2,3,4,6,11-hexahydro-1-naphthacenyl 2-(acetyloxy)-2-phenylethanoate
CAS No.:709640-12-0
Molecular Formula:C₃₀H₂₄O₁₀
Molecular Weight:544.515
Hs Code.:

Synonyms:3-acetyl-3,5,12-trihydroxy-6,11-dioxo-1,2,3,4,6,11-hexahydro-1-naphthacenyl 2-(acetyloxy)-2-phenylethanoate

Suppliers and Price of 3-acetyl-3,5,12-trihydroxy-6,11-dioxo-1,2,3,4,6,11-hexahydro-1-naphthacenyl 2-(acetyloxy)-2-phenylethanoate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 3-acetyl-3,5,12-trihydroxy-6,11-dioxo-1,2,3,4,6,11-hexahydro-1-naphthacenyl 2-(acetyloxy)-2-phenylethanoate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 3-acetyl-3,5,12-trihydroxy-6,11-dioxo-1,2,3,4,6,11-hexahydro-1-naphthacenyl 2-(acetyloxy)-2-phenylethanoate

There total 9 articles about 3-acetyl-3,5,12-trihydroxy-6,11-dioxo-1,2,3,4,6,11-hexahydro-1-naphthacenyl 2-(acetyloxy)-2-phenylethanoate 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: 47.0%

: 7322-88-5
(S)-acetylmandelic acid

: 60660-75-5,60733-78-0,63268-39-3,65877-42-1,70005-90-2,70005-91-3,74606-73-8,84773-46-6,58924-49-5
(+/-)-9-acetyl-6,7,9,11-tetrahydroxy-7,8,9,10-tetrahydronaphthacen-5,12-dione

: 709640-13-1
3-acetyl-3,5,12-trihydroxy-6,11-dioxo-1,2,3,4,6,11-hexahydro-1-naphthacenyl 2-(acetyloxy)-2-phenyl ethanoate

: 709640-12-0
3-acetyl-3,5,12-trihydroxy-6,11-dioxo-1,2,3,4,6,11-hexahydro-1-naphthacenyl 2-(acetyloxy)-2-phenylethanoate

Guidance literature:: With dmap; dicyclohexyl-carbodiimide; In dichloromethane; at 20 ℃; for 15h;
DOI:10.1081/SCC-120030758

Reference yield:

: 150-78-7
1,4-dimethoxybezene

: 709640-12-0
3-acetyl-3,5,12-trihydroxy-6,11-dioxo-1,2,3,4,6,11-hexahydro-1-naphthacenyl 2-(acetyloxy)-2-phenylethanoate

Guidance literature:: Multi-step reaction with 9 steps

1: 17 percent / AlCl₃ / CH₂Cl₂ / 4 h / 20 °C

2: 88 percent / triethylsilane; CF₃COOH / 0.5 h / 0 °C

3: 81 percent / tetrahydrofuran / 2 h / 0 °C

4: 85 percent / O₂; t-BuOK; P(OEt)3 / dimethylformamide / 1 h / -15 - -10 °C

5: 87 percent / AlCl₃ / nitrobenzene / 0 °C

6: 95 percent / p-TsOH / benzene / Heating

7: NBS; AIBN / CCl₄ / 0.5 h / Heating; irradiation

8: 0.11 g / aq. HCl / dioxane / 1 h / 80 °C

9: 47 percent / DMAP; DCC / CH₂Cl₂ / 15 h / 20 °C

With hydrogenchloride; triethylsilane; dmap; N-Bromosuccinimide; aluminium trichloride; 2,2'-azobis(isobutyronitrile); potassium tert-butylate; oxygen; toluene-4-sulfonic acid; dicyclohexyl-carbodiimide; trifluoroacetic acid; triethyl phosphite; In tetrahydrofuran; 1,4-dioxane; tetrachloromethane; dichloromethane; nitrobenzene; N,N-dimethyl-formamide; benzene; 1: Friedel-Crafts condensation;
DOI:10.1081/SCC-120030758

Reference yield:

: 33654-68-1,110881-09-9
1-(5,8-dimethoxy-1,2,3,4-tetrahydro-2-naphthalenyl)-1-ethanone

: 709640-12-0
3-acetyl-3,5,12-trihydroxy-6,11-dioxo-1,2,3,4,6,11-hexahydro-1-naphthacenyl 2-(acetyloxy)-2-phenylethanoate

Guidance literature:: Multi-step reaction with 6 steps

1: 85 percent / O₂; t-BuOK; P(OEt)3 / dimethylformamide / 1 h / -15 - -10 °C

2: 87 percent / AlCl₃ / nitrobenzene / 0 °C

3: 95 percent / p-TsOH / benzene / Heating

4: NBS; AIBN / CCl₄ / 0.5 h / Heating; irradiation

5: 0.11 g / aq. HCl / dioxane / 1 h / 80 °C

6: 47 percent / DMAP; DCC / CH₂Cl₂ / 15 h / 20 °C

With hydrogenchloride; dmap; N-Bromosuccinimide; aluminium trichloride; 2,2'-azobis(isobutyronitrile); potassium tert-butylate; oxygen; toluene-4-sulfonic acid; dicyclohexyl-carbodiimide; triethyl phosphite; In 1,4-dioxane; tetrachloromethane; dichloromethane; nitrobenzene; N,N-dimethyl-formamide; benzene;
DOI:10.1081/SCC-120030758