5-bromomethyl-2-chloro-N-(tricyclo[3.3.1.1^3,7]dec-1-ylmethyl)-benzamide

Base Information

Chemical Name:5-bromomethyl-2-chloro-N-(tricyclo[3.3.1.1^3,7]dec-1-ylmethyl)-benzamide
CAS No.:301672-76-4
Molecular Formula:C₁₉H₂₃BrClNO
Molecular Weight:396.755
Hs Code.:

5-bromomethyl-2-chloro-N-(tricyclo[3.3.1.1<sup>3,7</sup>]dec-1-ylmethyl)-benzamide

Synonyms:5-bromomethyl-2-chloro-N-(tricyclo[3.3.1.1^3,7]dec-1-ylmethyl)-benzamide

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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 5-bromomethyl-2-chloro-N-(tricyclo[3.3.1.1^3,7]dec-1-ylmethyl)-benzamide

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Technology Process of 5-bromomethyl-2-chloro-N-(tricyclo[3.3.1.1^3,7]dec-1-ylmethyl)-benzamide

There total 6 articles about 5-bromomethyl-2-chloro-N-(tricyclo[3.3.1.1^3,7]dec-1-ylmethyl)-benzamide 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:

: 66658-57-9
5-bromomethyl-2-chloro-benzoic acid

: 79-37-8
oxalyl dichloride

: 17768-41-1
adamantylmethylamine

: 301672-76-4
5-bromomethyl-2-chloro-N-(tricyclo[3.3.1.1^3,7]dec-1-ylmethyl)-benzamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In N-methyl-acetamide; dichloromethane;

Reference yield:

: C₈H₅OCl₂Br

: 17768-41-1
adamantylmethylamine

: 301672-76-4
5-bromomethyl-2-chloro-N-(tricyclo[3.3.1.1^3,7]dec-1-ylmethyl)-benzamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 ℃; for 0.25h;
DOI:10.1021/jm700949w

Reference yield:

: 17768-41-1
adamantylmethylamine

: 301672-76-4
5-bromomethyl-2-chloro-N-(tricyclo[3.3.1.1^3,7]dec-1-ylmethyl)-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 22 h / 20 °C / Inert atmosphere

2: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / chloroform / 4 h / Reflux; Inert atmosphere

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane; chloroform;
DOI:10.1002/cmdc.202000303