tert-butyl decylcarbamate

Base Information

Chemical Name:tert-butyl decylcarbamate
CAS No.:1025502-64-0
Molecular Formula:C₁₅H₃₁NO₂
Molecular Weight:257.417
Hs Code.:

Synonyms:tert-butyl decylcarbamate

Suppliers and Price of tert-butyl decylcarbamate

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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 tert-butyl decylcarbamate

Chemical Property:

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Technology Process of tert-butyl decylcarbamate

There total 4 articles about tert-butyl decylcarbamate 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: 100.0%

: 2016-57-1
1-aminodecane

: 24424-99-5
di-tert-butyl dicarbonate

: 1025502-64-0
tert-butyl decylcarbamate

Guidance literature:: With 1-methylimidazolium tetrafluoroborate; at 30 - 35 ℃; for 0.333333h;
DOI:10.1016/j.tetlet.2008.02.126

Reference yield:

: 1975-78-6
n-decanenitrile

: 24424-99-5
di-tert-butyl dicarbonate

: 1025502-64-0
tert-butyl decylcarbamate

: 1070-01-5
tri(n-decyl)amine

Guidance literature:: n-decanenitrile; With 10% rhodium on carbon; hydrogen; In toluene; at 90 ℃; Flow reactor;

di-tert-butyl dicarbonate; With triethylamine; In 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran; Solvent;
DOI:10.1002/cssc.202102138

Reference yield:

: 1975-78-6
n-decanenitrile

: 24424-99-5
di-tert-butyl dicarbonate

: 1025502-64-0
tert-butyl decylcarbamate

: 621-77-2
tripentylamine

Guidance literature:: n-decanenitrile; With 10% rhodium on carbon; hydrogen; In acetic acid; at 90 ℃; Flow reactor;

di-tert-butyl dicarbonate; With triethylamine; In 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran; Reagent/catalyst; Concentration; Solvent; Catalytic behavior;
DOI:10.1002/cssc.202102138