6-benzyl-3,9-dimethoxy-1,2-methylenedioxy-10,11-methylenedioxy-6,7-dihydro-5H-dibenz[c,e]azepine

Base Information

Chemical Name:6-benzyl-3,9-dimethoxy-1,2-methylenedioxy-10,11-methylenedioxy-6,7-dihydro-5H-dibenz[c,e]azepine
CAS No.:1376611-66-3
Molecular Formula:C₂₅H₂₃NO₆
Molecular Weight:433.461
Hs Code.:

Synonyms:6-benzyl-3,9-dimethoxy-1,2-methylenedioxy-10,11-methylenedioxy-6,7-dihydro-5H-dibenz[c,e]azepine

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

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Chemical Property of 6-benzyl-3,9-dimethoxy-1,2-methylenedioxy-10,11-methylenedioxy-6,7-dihydro-5H-dibenz[c,e]azepine

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Technology Process of 6-benzyl-3,9-dimethoxy-1,2-methylenedioxy-10,11-methylenedioxy-6,7-dihydro-5H-dibenz[c,e]azepine

There total 1 articles about 6-benzyl-3,9-dimethoxy-1,2-methylenedioxy-10,11-methylenedioxy-6,7-dihydro-5H-dibenz[c,e]azepine 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: 81.0%

: 1376611-75-4
7,7'-dimethoxy-[4,4'-dibenzo[d][1,3]dioxo]-5,5'-bis(methylene)dimethylsulfonate

: 100-46-9
benzylamine

: 1376611-66-3
6-benzyl-3,9-dimethoxy-1,2-methylenedioxy-10,11-methylenedioxy-6,7-dihydro-5H-dibenz[c,e]azepine

Guidance literature:: With triethylamine; In acetonitrile; at 40 ℃;
DOI:10.1016/j.ejmech.2012.02.034

Reference yield: 41.0%

: 1376611-66-3
6-benzyl-3,9-dimethoxy-1,2-methylenedioxy-10,11-methylenedioxy-6,7-dihydro-5H-dibenz[c,e]azepine

: 1376611-74-3
6-benzyl-3,9-dimethoxy-1,2-methylenedioxy-10,11-methylenedioxy-6,7-dihydro-dibenz[c,e]azepine-5-one

Guidance literature:: With potassium permanganate; cetyltrimethylammonim bromide; In dichloromethane; Reflux;
DOI:10.1016/j.ejmech.2012.02.034