methyl 3-(2-(naphthalen-1-ylmethylcarbamoyl)-4-(phenoxymethyl)phenyl)propanoate

Base Information

Chemical Name:methyl 3-(2-(naphthalen-1-ylmethylcarbamoyl)-4-(phenoxymethyl)phenyl)propanoate
CAS No.:1616088-61-9
Molecular Formula:C₂₉H₂₇NO₄
Molecular Weight:453.538
Hs Code.:

Synonyms:methyl 3-(2-(naphthalen-1-ylmethylcarbamoyl)-4-(phenoxymethyl)phenyl)propanoate

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Chemical Property of methyl 3-(2-(naphthalen-1-ylmethylcarbamoyl)-4-(phenoxymethyl)phenyl)propanoate

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Technology Process of methyl 3-(2-(naphthalen-1-ylmethylcarbamoyl)-4-(phenoxymethyl)phenyl)propanoate

There total 1 articles about methyl 3-(2-(naphthalen-1-ylmethylcarbamoyl)-4-(phenoxymethyl)phenyl)propanoate 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: 64.0%

: 67-56-1
methanol

: 118-31-0
(naphth-1-yl)methylamine

: 1616088-58-4
2-(2-carboxyethyl)-5-(phenoxymethyl)benzoic Acid

: 1616088-61-9
methyl 3-(2-(naphthalen-1-ylmethylcarbamoyl)-4-(phenoxymethyl)phenyl)propanoate

Guidance literature:: methanol; 2-(2-carboxyethyl)-5-(phenoxymethyl)benzoic Acid; With sulfuric acid; for 0.333333h; Schlenk technique;

(naphth-1-yl)methylamine; With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 0 - 20 ℃; Inert atmosphere; Schlenk technique;
DOI:10.1021/jo5008465

Reference yield: 62.0%

: 1616088-61-9
methyl 3-(2-(naphthalen-1-ylmethylcarbamoyl)-4-(phenoxymethyl)phenyl)propanoate

: 499146-71-3
3-[2-{[(1-naphthylmethyl)amino]carbonyl}-4-(phenoxymethyl)phenyl]propanoic acid

Guidance literature:: With lithium hydroxide monohydrate; In tetrahydrofuran; methanol; at 60 ℃; for 4h; Schlenk technique;
DOI:10.1021/jo5008465