(+/-)-2,8-dimethyl-5-(2-oxo-2-phenyl-ethyl)-6H,12H-5,11-methano-dibenzo[b,f][1,5]diazocin-5-ium bromide

Base Information

Chemical Name:(+/-)-2,8-dimethyl-5-(2-oxo-2-phenyl-ethyl)-6H,12H-5,11-methano-dibenzo[b,f][1,5]diazocin-5-ium bromide
CAS No.:1190482-38-2
Molecular Formula:Br*C₂₅H₂₅N₂O
Molecular Weight:449.39
Hs Code.:

Synonyms:(+/-)-2,8-dimethyl-5-(2-oxo-2-phenyl-ethyl)-6H,12H-5,11-methano-dibenzo[b,f][1,5]diazocin-5-ium bromide

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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 (+/-)-2,8-dimethyl-5-(2-oxo-2-phenyl-ethyl)-6H,12H-5,11-methano-dibenzo[b,f][1,5]diazocin-5-ium bromide

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Technology Process of (+/-)-2,8-dimethyl-5-(2-oxo-2-phenyl-ethyl)-6H,12H-5,11-methano-dibenzo[b,f][1,5]diazocin-5-ium bromide

There total 1 articles about (+/-)-2,8-dimethyl-5-(2-oxo-2-phenyl-ethyl)-6H,12H-5,11-methano-dibenzo[b,f][1,5]diazocin-5-ium bromide 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: 87.0%

: 529-81-7
Troeger's base

: 70-11-1
α-bromoacetophenone

: 1190482-38-2
(+/-)-2,8-dimethyl-5-(2-oxo-2-phenyl-ethyl)-6H,12H-5,11-methano-dibenzo[b,f][1,5]diazocin-5-ium bromide

Guidance literature:: In benzene; for 12h; Inert atmosphere; Reflux;
DOI:10.1039/b925065d

Reference yield: 85.0%

: 1190482-38-2
(+/-)-2,8-dimethyl-5-(2-oxo-2-phenyl-ethyl)-6H,12H-5,11-methano-dibenzo[b,f][1,5]diazocin-5-ium bromide

: 1225379-24-7
2-(2,8-dimethyl-11,12-dihydro-6H-dibenzo[b,f][1,5]diazocin-5-yl)-1-phenyl-ethanone

: (+/-)-2,8-dimethyl-6H,12H-5,11-[benzoyl-ethano]-dibenzo[b,f][1,5]diazocine

Guidance literature:: With aluminum oxide; In chloroform; at 25 ℃; for 2.5h; diastereoselective reaction; Inert atmosphere;
DOI:10.1039/b925065d