2-[(2-ethoxycarbonyl-phenylamino)-methylene]-malonic acid diethyl ester

Base Information

Chemical Name:2-[(2-ethoxycarbonyl-phenylamino)-methylene]-malonic acid diethyl ester
CAS No.:1415327-36-4
Molecular Formula:C₁₇H₂₁NO₆
Molecular Weight:335.357
Hs Code.:

Synonyms:2-[(2-ethoxycarbonyl-phenylamino)-methylene]-malonic acid diethyl ester

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Chemical Property of 2-[(2-ethoxycarbonyl-phenylamino)-methylene]-malonic acid diethyl ester

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Technology Process of 2-[(2-ethoxycarbonyl-phenylamino)-methylene]-malonic acid diethyl ester

There total 2 articles about 2-[(2-ethoxycarbonyl-phenylamino)-methylene]-malonic acid diethyl ester 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: 80.0%

: 74-96-4
ethyl bromide

: 52693-18-2
2-[(2-carboxy-phenylamino)-methylene]-malonic acid diethyl ester

: 1415327-36-4
2-[(2-ethoxycarbonyl-phenylamino)-methylene]-malonic acid diethyl ester

Guidance literature:: 2-[(2-carboxy-phenylamino)-methylene]-malonic acid diethyl ester; With potassium carbonate; In acetone; for 1h;

ethyl bromide; In acetone; for 24h;
DOI:10.1055/s-0031-1290449

Reference yield:

: 87-13-8
diethyl 2-ethoxymethylenemalonate

: 87-25-2
2-ethoxycarbonylaniline

: 1415327-36-4
2-[(2-ethoxycarbonyl-phenylamino)-methylene]-malonic acid diethyl ester

Guidance literature:: In ethanol; at 22.84 ℃;
DOI:10.1039/c4ce02125h

Reference yield: 81.0%

: 1415327-36-4
2-[(2-ethoxycarbonyl-phenylamino)-methylene]-malonic acid diethyl ester

: 1415327-40-0
2-[(2-ethoxycarbonyl-phenylamino)-methylene]-malonic acid monoethyl ester

Guidance literature:: With boron trifluoride diethyl etherate; In chloroform; at 20 ℃; for 1.2h; chemoselective reaction; Inert atmosphere;
DOI:10.1055/s-0031-1290449