2-(4-((4-((Tert-butoxycarbonylamino)methyl)benzamido) methyl)phenoxy)acetic acid

Base Information

Chemical Name:2-(4-((4-((Tert-butoxycarbonylamino)methyl)benzamido) methyl)phenoxy)acetic acid
CAS No.:1290056-32-4
Molecular Formula:C₂₂H₂₆N₂O₆
Molecular Weight:414.458
Hs Code.:

Synonyms:2-(4-((4-((Tert-butoxycarbonylamino)methyl)benzamido) methyl)phenoxy)acetic acid

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Chemical Property of 2-(4-((4-((Tert-butoxycarbonylamino)methyl)benzamido) methyl)phenoxy)acetic acid

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Technology Process of 2-(4-((4-((Tert-butoxycarbonylamino)methyl)benzamido) methyl)phenoxy)acetic acid

There total 7 articles about 2-(4-((4-((Tert-butoxycarbonylamino)methyl)benzamido) methyl)phenoxy)acetic acid 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: 82.6%

: 1290056-31-3
ethyl 2-(4-((4-(((tert-butoxycarbonyl)amino)methyl)benzamido) methyl)phenoxy)acetate

: 1290056-32-4
2-(4-((4-((Tert-butoxycarbonylamino)methyl)benzamido) methyl)phenoxy)acetic acid

Guidance literature:: ethyl 2-(4-((4-(((tert-butoxycarbonyl)amino)methyl)benzamido) methyl)phenoxy)acetate; With lithium hydroxide monohydrate; water; In tetrahydrofuran; at 0 - 20 ℃; for 2h;

With hydrogenchloride; In water; at 0 ℃;

Reference yield:

: 767-00-0
4-cyanophenol

: 1290056-32-4
2-(4-((4-((Tert-butoxycarbonylamino)methyl)benzamido) methyl)phenoxy)acetic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / acetone / 12 h / Reflux

2.1: hydrogen; acetic acid / 10% palladium on charcoal / ethanol / 24 h / 5171.62 Torr

3.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 0.25 h / 0 - 20 °C / Inert atmosphere

3.2: 0.33 h / 0 - 20 °C

4.1: water; lithium hydroxide monohydrate / tetrahydrofuran / 2 h / 0 - 20 °C

4.2: 0 °C

With lithium hydroxide monohydrate; water; hydrogen; potassium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; HATU; 10% palladium on charcoal; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; acetone;

Reference yield:

: 30041-95-3
ethyl (4-cyano-phenoxy)-acetate

: 1290056-32-4
2-(4-((4-((Tert-butoxycarbonylamino)methyl)benzamido) methyl)phenoxy)acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogen; acetic acid / 10% palladium on charcoal / ethanol / 24 h / 5171.62 Torr

2.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 0.25 h / 0 - 20 °C / Inert atmosphere

2.2: 0.33 h / 0 - 20 °C

3.1: water; lithium hydroxide monohydrate / tetrahydrofuran / 2 h / 0 - 20 °C

3.2: 0 °C

With lithium hydroxide monohydrate; water; hydrogen; acetic acid; N-ethyl-N,N-diisopropylamine; HATU; 10% palladium on charcoal; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide;