tert-butyl 2-((3-(4-((1E,4E)-5-(4-(dimethylamino)phenyl)-3-oxopenta-1,4-dienyl)phenoxy)propyl)(2-(tritylthio)ethyl)amino)ethyl(2-(tritylthio)ethyl)carbamate

Base Information

Chemical Name:tert-butyl 2-((3-(4-((1E,4E)-5-(4-(dimethylamino)phenyl)-3-oxopenta-1,4-dienyl)phenoxy)propyl)(2-(tritylthio)ethyl)amino)ethyl(2-(tritylthio)ethyl)carbamate
CAS No.:1444512-35-9
Molecular Formula:C₇₁H₇₅N₃O₄S₂
Molecular Weight:1098.53
Hs Code.:

tert-butyl 2-((3-(4-((1E,4E)-5-(4-(dimethylamino)phenyl)-3-oxopenta-1,4-dienyl)phenoxy)propyl)(2-(tritylthio)ethyl)amino)ethyl(2-(tritylthio)ethyl)carbamate

Synonyms:tert-butyl 2-((3-(4-((1E,4E)-5-(4-(dimethylamino)phenyl)-3-oxopenta-1,4-dienyl)phenoxy)propyl)(2-(tritylthio)ethyl)amino)ethyl(2-(tritylthio)ethyl)carbamate

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Chemical Property of tert-butyl 2-((3-(4-((1E,4E)-5-(4-(dimethylamino)phenyl)-3-oxopenta-1,4-dienyl)phenoxy)propyl)(2-(tritylthio)ethyl)amino)ethyl(2-(tritylthio)ethyl)carbamate

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Technology Process of tert-butyl 2-((3-(4-((1E,4E)-5-(4-(dimethylamino)phenyl)-3-oxopenta-1,4-dienyl)phenoxy)propyl)(2-(tritylthio)ethyl)amino)ethyl(2-(tritylthio)ethyl)carbamate

There total 2 articles about tert-butyl 2-((3-(4-((1E,4E)-5-(4-(dimethylamino)phenyl)-3-oxopenta-1,4-dienyl)phenoxy)propyl)(2-(tritylthio)ethyl)amino)ethyl(2-(tritylthio)ethyl)carbamate 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:

: 17954-81-3
4-(3-bromopropoxy)benzaldehyde

: 1444512-35-9
tert-butyl 2-((3-(4-((1E,4E)-5-(4-(dimethylamino)phenyl)-3-oxopenta-1,4-dienyl)phenoxy)propyl)(2-(tritylthio)ethyl)amino)ethyl(2-(tritylthio)ethyl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium methylate / ethanol / 20 °C

2: potassium carbonate / acetonitrile / 48 h / 90 °C

With sodium methylate; potassium carbonate; In ethanol; acetonitrile; 1: |Claisen Condensation;
DOI:10.1016/j.ejmech.2013.03.057

Reference yield:

: 123-08-0,65581-83-1
4-hydroxy-benzaldehyde

: 1444512-35-9
tert-butyl 2-((3-(4-((1E,4E)-5-(4-(dimethylamino)phenyl)-3-oxopenta-1,4-dienyl)phenoxy)propyl)(2-(tritylthio)ethyl)amino)ethyl(2-(tritylthio)ethyl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / acetonitrile / 12 h / 90 °C

2: sodium methylate / ethanol / 20 °C

3: potassium carbonate / acetonitrile / 48 h / 90 °C

With sodium methylate; potassium carbonate; In ethanol; acetonitrile; 2: |Claisen Condensation;
DOI:10.1016/j.ejmech.2013.03.057

Reference yield:

: 1444512-35-9
tert-butyl 2-((3-(4-((1E,4E)-5-(4-(dimethylamino)phenyl)-3-oxopenta-1,4-dienyl)phenoxy)propyl)(2-(tritylthio)ethyl)amino)ethyl(2-(tritylthio)ethyl)carbamate

: C₂₈H₃₆N₃O₃S₂⁽⁹⁹⁾Tc

Guidance literature:: tert-butyl 2-((3-(4-((1E,4E)-5-(4-(dimethylamino)phenyl)-3-oxopenta-1,4-dienyl)phenoxy)propyl)(2-(tritylthio)ethyl)amino)ethyl(2-(tritylthio)ethyl)carbamate; With triethylsilane; trifluoroacetic acid; at 20 ℃; for 0.166667h; Inert atmosphere;

In ethanol; at 100 ℃; for 0.166667h;
DOI:10.1016/j.ejmech.2013.03.057