3,5-O-(3,4-dimethoxybenzylidene)-9,11-O-(2,4,6-trimethylbenzylidene)-(9S)-9-dihydroerythronolide A

Base Information

Chemical Name:3,5-O-(3,4-dimethoxybenzylidene)-9,11-O-(2,4,6-trimethylbenzylidene)-(9S)-9-dihydroerythronolide A
CAS No.:124648-35-7
Molecular Formula:C₄₀H₅₈O₁₀
Molecular Weight:698.895
Hs Code.:

Synonyms:3,5-O-(3,4-dimethoxybenzylidene)-9,11-O-(2,4,6-trimethylbenzylidene)-(9S)-9-dihydroerythronolide A

Suppliers and Price of 3,5-O-(3,4-dimethoxybenzylidene)-9,11-O-(2,4,6-trimethylbenzylidene)-(9S)-9-dihydroerythronolide A

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 3,5-O-(3,4-dimethoxybenzylidene)-9,11-O-(2,4,6-trimethylbenzylidene)-(9S)-9-dihydroerythronolide A

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 3,5-O-(3,4-dimethoxybenzylidene)-9,11-O-(2,4,6-trimethylbenzylidene)-(9S)-9-dihydroerythronolide A

There total 11 articles about 3,5-O-(3,4-dimethoxybenzylidene)-9,11-O-(2,4,6-trimethylbenzylidene)-(9S)-9-dihydroerythronolide A 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: 98.0%

: 123388-01-2,124648-34-6
3,5-O-(3,4-dimethoxybenzylidene)-9,11-O-(2,4,6-trimethylbenzylidene)-(9S)-9-dihydroerythronolide A seco-acid

: 124648-35-7
3,5-O-(3,4-dimethoxybenzylidene)-9,11-O-(2,4,6-trimethylbenzylidene)-(9S)-9-dihydroerythronolide A

Guidance literature:: With dmap; 2,4,6-trichlorobenzoyl chloride; triethylamine; In benzene; for 1h; Ambient temperature;
DOI:10.1248/cpb.40.2540

Reference yield: 98.0%

: 123388-01-2,124648-34-6
3,5-O-(3,4-dimethoxybenzylidene)-9,11-O-(2,4,6-trimethylbenzylidene)-(9S)-9-dihydroerythronolide A seco-acid

: 123367-30-6,124648-35-7
(1S,2R,4R,5R,7R,9S,10R,13R,14R,15S,17R,19S,20S)-7-(3,4-Dimethoxy-phenyl)-13-ethyl-4,14-dihydroxy-2,4,10,14,19,20-hexamethyl-17-(2,4,6-trimethyl-phenyl)-6,8,12,16,18-pentaoxa-tricyclo[13.3.1.1^5,9]icosan-11-one

Guidance literature:: With dmap; 2,4,6-trichlorobenzoyl chloride; triethylamine; In benzene; for 1h; Ambient temperature;
DOI:10.1016/S0040-4039(00)97066-7

Reference yield:

: 131755-84-5
C₄₈H₆₈O₁₂

: 123367-30-6,124648-35-7
3,5-O-(3,4-Dimethoxybenzylidene)-9,11-O-(2,4,6-trimethylbenzylidene)-(9S)-9-dihydroerythronolide A

Guidance literature:: Multi-step reaction with 4 steps

1: 50 percent / diethyl ether / 0.05 h / Ambient temperature

2: 80 percent / H₂ / 10percent Pd/C / ethanol / 0.33 h / Ambient temperature

3: 94 percent / 3N NaOH / methanol / 18 h / Ambient temperature

4: 1.) Et₃N, 2.) 4-dimethylaminopyridine / 1.) toluene, room temp., 48 h , 2.) 50 min

With dmap; sodium hydroxide; hydrogen; triethylamine; palladium on activated charcoal; In methanol; diethyl ether; ethanol;
DOI:10.1016/S0040-4020(01)85585-X