ethyl 4-[N-(naphthalen-2-ylmethyl)-N-(5,6,7,8-tetrahydro-5,5,8,8-tetramethylnaphthalen-2-yl)amino]benzoate

Base Information

Chemical Name:ethyl 4-[N-(naphthalen-2-ylmethyl)-N-(5,6,7,8-tetrahydro-5,5,8,8-tetramethylnaphthalen-2-yl)amino]benzoate
CAS No.:1300118-23-3
Molecular Formula:C₃₄H₃₇NO₂
Molecular Weight:491.673
Hs Code.:

Synonyms:ethyl 4-[N-(naphthalen-2-ylmethyl)-N-(5,6,7,8-tetrahydro-5,5,8,8-tetramethylnaphthalen-2-yl)amino]benzoate

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Chemical Property of ethyl 4-[N-(naphthalen-2-ylmethyl)-N-(5,6,7,8-tetrahydro-5,5,8,8-tetramethylnaphthalen-2-yl)amino]benzoate

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Technology Process of ethyl 4-[N-(naphthalen-2-ylmethyl)-N-(5,6,7,8-tetrahydro-5,5,8,8-tetramethylnaphthalen-2-yl)amino]benzoate

There total 2 articles about ethyl 4-[N-(naphthalen-2-ylmethyl)-N-(5,6,7,8-tetrahydro-5,5,8,8-tetramethylnaphthalen-2-yl)amino]benzoate 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: 99.0%

: 214694-10-7
4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-ylamino)-benzoic acid ethyl ester

: 1300118-23-3
ethyl 4-[N-(naphthalen-2-ylmethyl)-N-(5,6,7,8-tetrahydro-5,5,8,8-tetramethylnaphthalen-2-yl)amino]benzoate

Guidance literature:: 4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-ylamino)-benzoic acid ethyl ester; With sodium hydride; In N,N-dimethyl-formamide; for 0.333333h; Inert atmosphere;

naphthalen-2-ylmethyl halide; In N,N-dimethyl-formamide; at 20 ℃; Inert atmosphere;
DOI:10.1016/j.bmc.2011.03.026

Reference yield:

: 51934-41-9
4-iodobenzoic acid ethyl ester

: 1300118-23-3
ethyl 4-[N-(naphthalen-2-ylmethyl)-N-(5,6,7,8-tetrahydro-5,5,8,8-tetramethylnaphthalen-2-yl)amino]benzoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate / toluene

2.1: sodium hydride / N,N-dimethyl-formamide / 0.33 h / Inert atmosphere

2.2: 20 °C / Inert atmosphere

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; sodium hydride; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate; In N,N-dimethyl-formamide; toluene;
DOI:10.1016/j.bmc.2011.03.026

Reference yield: 100.0%

: 1300118-23-3
ethyl 4-[N-(naphthalen-2-ylmethyl)-N-(5,6,7,8-tetrahydro-5,5,8,8-tetramethylnaphthalen-2-yl)amino]benzoate

: 214693-79-5
4-[N-(naphthalen-2-ylmethyl)-N-(5,6,7,8-tetrahydro-5,5,8,8-tetramethylnaphthalen-2-yl)amino]benzoic acid

Guidance literature:: ethyl 4-[N-(naphthalen-2-ylmethyl)-N-(5,6,7,8-tetrahydro-5,5,8,8-tetramethylnaphthalen-2-yl)amino]benzoate; With potassium hydroxide; In ethanol; water; at 20 ℃;

With hydrogenchloride; In ethanol; water;
DOI:10.1016/j.bmc.2011.03.026