1-carbomethoxy-4'-<<4-<<(tert-butyloxy)ethyl>oxy>phenyl>ethynyl>biphenyl

Base Information

Chemical Name:1-carbomethoxy-4'-<<4-<<(tert-butyloxy)ethyl>oxy>phenyl>ethynyl>biphenyl
CAS No.:158937-14-5
Molecular Formula:C₂₈H₂₈O₄
Molecular Weight:428.528
Hs Code.:

Synonyms:1-carbomethoxy-4'-<<4-<<(tert-butyloxy)ethyl>oxy>phenyl>ethynyl>biphenyl

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Chemical Property of 1-carbomethoxy-4'-<<4-<<(tert-butyloxy)ethyl>oxy>phenyl>ethynyl>biphenyl

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Technology Process of 1-carbomethoxy-4'-<<4-<<(tert-butyloxy)ethyl>oxy>phenyl>ethynyl>biphenyl

There total 5 articles about 1-carbomethoxy-4'-<<4-<<(tert-butyloxy)ethyl>oxy>phenyl>ethynyl>biphenyl 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: 90.0%

: 108366-80-9
2-(tert-butoxy)ethyl 4-methylbenzenesulfonate

: 158937-21-4
1-carbomethoxy-4'-<(4-hydroxyphenyl)ethynyl>biphenyl

: 158937-14-5
1-carbomethoxy-4'-<<4-<<(tert-butyloxy)ethyl>oxy>phenyl>ethynyl>biphenyl

Guidance literature:: With tert-butoxide; In acetonitrile; for 17h; Heating;
DOI:10.1021/jm00017a012

Reference yield:

: 540-38-5
p-Iodophenol

: 158937-14-5
1-carbomethoxy-4'-<<4-<<(tert-butyloxy)ethyl>oxy>phenyl>ethynyl>biphenyl

Guidance literature:: Multi-step reaction with 2 steps

1: 81 percent / Et₃N, PdCl₂, triphenylphosphine, CuI / acetonitrile / 3 h / Heating

2: 90 percent / tert-butoxide / acetonitrile / 17 h / Heating

With copper(l) iodide; tert-butoxide; triethylamine; triphenylphosphine; palladium dichloride; In acetonitrile;
DOI:10.1021/jm00017a012

Reference yield:

: 158937-83-8
methyl 4'-ethynyl-[1,1'-biphenyl]-4-carboxylate

: 158937-14-5
1-carbomethoxy-4'-<<4-<<(tert-butyloxy)ethyl>oxy>phenyl>ethynyl>biphenyl

Guidance literature:: Multi-step reaction with 2 steps

1: 81 percent / Et₃N, PdCl₂, triphenylphosphine, CuI / acetonitrile / 3 h / Heating

2: 90 percent / tert-butoxide / acetonitrile / 17 h / Heating

With copper(l) iodide; tert-butoxide; triethylamine; triphenylphosphine; palladium dichloride; In acetonitrile;
DOI:10.1021/jm00017a012