tert-butyl (4-((1E,4E)-5-(4-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)phenyl)-3-oxopenta-1,4-dien-1-yl)phenyl)(methyl)carbamate

Base Information

Chemical Name:tert-butyl (4-((1E,4E)-5-(4-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)phenyl)-3-oxopenta-1,4-dien-1-yl)phenyl)(methyl)carbamate
CAS No.:1285534-64-6
Molecular Formula:C₂₉H₃₇NO₇
Molecular Weight:511.615
Hs Code.:

Synonyms:tert-butyl (4-((1E,4E)-5-(4-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)phenyl)-3-oxopenta-1,4-dien-1-yl)phenyl)(methyl)carbamate

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Chemical Property of tert-butyl (4-((1E,4E)-5-(4-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)phenyl)-3-oxopenta-1,4-dien-1-yl)phenyl)(methyl)carbamate

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Technology Process of tert-butyl (4-((1E,4E)-5-(4-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)phenyl)-3-oxopenta-1,4-dien-1-yl)phenyl)(methyl)carbamate

There total 7 articles about tert-butyl (4-((1E,4E)-5-(4-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)phenyl)-3-oxopenta-1,4-dien-1-yl)phenyl)(methyl)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: 85.0%

: 1285534-63-5
tert-butyl methyl(4-((1E,4E)-3-oxo-5-(4-((2,2,3,3-tetramethyl-4,7,10-trioxa-3-siladodecan-12-yl)oxy)phenyl)penta-1,4-dien-1-yl)phenyl)carbamate

: 1285534-64-6
tert-butyl (4-((1E,4E)-5-(4-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)phenyl)-3-oxopenta-1,4-dien-1-yl)phenyl)(methyl)carbamate

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 2h;
DOI:10.1021/jm101404k

Reference yield:

: 1285534-36-2
(E)-4-(4-(methylamino)phenyl)but-3-en-2-one

: 1285534-64-6
tert-butyl (4-((1E,4E)-5-(4-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)phenyl)-3-oxopenta-1,4-dien-1-yl)phenyl)(methyl)carbamate

Guidance literature:: Multi-step reaction with 4 steps

1: sodium methylate / methanol; ethanol / 12 h / 20 °C

2: 1H-imidazole / dichloromethane / 2 h / 20 °C

3: tetrahydrofuran / 48 h / Inert atmosphere; Reflux

4: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C

With 1H-imidazole; tetrabutyl ammonium fluoride; sodium methylate; In tetrahydrofuran; methanol; ethanol; dichloromethane; 1: Claisen condensation;
DOI:10.1021/jm101404k

Reference yield:

: 946-49-6,3490-37-7,30625-98-0
(E)-4-(4-nitrophenyl)-3-buten-2-one

: 1285534-64-6
tert-butyl (4-((1E,4E)-5-(4-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)phenyl)-3-oxopenta-1,4-dien-1-yl)phenyl)(methyl)carbamate

Guidance literature:: Multi-step reaction with 6 steps

1: hydrogenchloride; tin(ll) chloride / ethanol; water / 2 h / Reflux

2: potassium carbonate / acetone / 8 h / 20 °C

3: sodium methylate / methanol; ethanol / 12 h / 20 °C

4: 1H-imidazole / dichloromethane / 2 h / 20 °C

5: tetrahydrofuran / 48 h / Inert atmosphere; Reflux

6: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C

With 1H-imidazole; hydrogenchloride; tetrabutyl ammonium fluoride; sodium methylate; potassium carbonate; tin(ll) chloride; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; acetone; 3: Claisen condensation;
DOI:10.1021/jm101404k