7,16-Bis-(4'-heptyl-biphenyl-4-ylmethyl)-1,4,10,13-tetraoxa-7,16-diaza-cyclooctadecane

Base Information

Chemical Name:7,16-Bis-(4'-heptyl-biphenyl-4-ylmethyl)-1,4,10,13-tetraoxa-7,16-diaza-cyclooctadecane
CAS No.:124513-34-4
Molecular Formula:C₅₂H₇₄N₂O₄
Molecular Weight:791.171
Hs Code.:

Synonyms:7,16-Bis-(4'-heptyl-biphenyl-4-ylmethyl)-1,4,10,13-tetraoxa-7,16-diaza-cyclooctadecane

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Chemical Property of 7,16-Bis-(4'-heptyl-biphenyl-4-ylmethyl)-1,4,10,13-tetraoxa-7,16-diaza-cyclooctadecane

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Technology Process of 7,16-Bis-(4'-heptyl-biphenyl-4-ylmethyl)-1,4,10,13-tetraoxa-7,16-diaza-cyclooctadecane

There total 3 articles about 7,16-Bis-(4'-heptyl-biphenyl-4-ylmethyl)-1,4,10,13-tetraoxa-7,16-diaza-cyclooctadecane 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: 70.0%

: 124513-32-2
[16-(4'-Heptyl-biphenyl-4-carbonyl)-1,4,10,13-tetraoxa-7,16-diaza-cyclooctadec-7-yl]-(4'-heptyl-biphenyl-4-yl)-methanone

: 124513-34-4
7,16-Bis-(4'-heptyl-biphenyl-4-ylmethyl)-1,4,10,13-tetraoxa-7,16-diaza-cyclooctadecane

Guidance literature:: With diborane; In tetrahydrofuran;
DOI:10.1021/jo00289a028

Reference yield:

: 58573-87-8
4'-heptylbiphenyl-4-ylcarboxylic acid chloride

: 124513-34-4
7,16-Bis-(4'-heptyl-biphenyl-4-ylmethyl)-1,4,10,13-tetraoxa-7,16-diaza-cyclooctadecane

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / Et₃N / CH₂Cl₂ / 5 h / Heating

2: 70 percent / B₂H₆ / tetrahydrofuran

With triethylamine; diborane; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jo00289a028

Reference yield:

: 58573-94-7
4-(4-heptylphenyl)benzoic acid

: 124513-34-4
7,16-Bis-(4'-heptyl-biphenyl-4-ylmethyl)-1,4,10,13-tetraoxa-7,16-diaza-cyclooctadecane

Guidance literature:: Multi-step reaction with 3 steps

1: SOCl₂

2: 76 percent / Et₃N / CH₂Cl₂ / 5 h / Heating

3: 70 percent / B₂H₆ / tetrahydrofuran

With thionyl chloride; triethylamine; diborane; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jo00289a028