tert-butyl 2-(3-allyl-3-(2-(but-3-enyloxy)benzoyl)ureido)benzylcarbamate

Base Information

Chemical Name:tert-butyl 2-(3-allyl-3-(2-(but-3-enyloxy)benzoyl)ureido)benzylcarbamate
CAS No.:1269142-31-5
Molecular Formula:C₂₇H₃₃N₃O₅
Molecular Weight:479.576
Hs Code.:

Synonyms:tert-butyl 2-(3-allyl-3-(2-(but-3-enyloxy)benzoyl)ureido)benzylcarbamate

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Chemical Property of tert-butyl 2-(3-allyl-3-(2-(but-3-enyloxy)benzoyl)ureido)benzylcarbamate

Chemical Property:

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Technology Process of tert-butyl 2-(3-allyl-3-(2-(but-3-enyloxy)benzoyl)ureido)benzylcarbamate

There total 7 articles about tert-butyl 2-(3-allyl-3-(2-(but-3-enyloxy)benzoyl)ureido)benzylcarbamate 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:

: C₁₅H₁₆ClNO₃

: 162046-50-6
tert-butyl 2-aminobenzylcarbamate

: 1269142-31-5
tert-butyl 2-(3-allyl-3-(2-(but-3-enyloxy)benzoyl)ureido)benzylcarbamate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In acetonitrile; at 0 - 20 ℃; for 0.25h;
DOI:10.1039/c0ob00723d

Reference yield:

: 1269142-18-8
N-allyl-2-(but-3-enyloxy)benzamide

: 1269142-31-5
tert-butyl 2-(3-allyl-3-(2-(but-3-enyloxy)benzoyl)ureido)benzylcarbamate

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / diethyl ether / 0.75 h

2: diethyl ether; toluene / 1 h / 0 - 20 °C

3: N-ethyl-N,N-diisopropylamine / acetonitrile / 0.25 h / 0 - 20 °C

With triethylamine; N-ethyl-N,N-diisopropylamine; In diethyl ether; toluene; acetonitrile;
DOI:10.1039/c0ob00723d

Reference yield:

: C₁₇H₂₅NO₂Si

: 1269142-31-5
tert-butyl 2-(3-allyl-3-(2-(but-3-enyloxy)benzoyl)ureido)benzylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: diethyl ether; toluene / 1 h / 0 - 20 °C

2: N-ethyl-N,N-diisopropylamine / acetonitrile / 0.25 h / 0 - 20 °C

With N-ethyl-N,N-diisopropylamine; In diethyl ether; toluene; acetonitrile;
DOI:10.1039/c0ob00723d