2-{4-[2-(4-Chloro-benzoylamino)-acetylamino]-phenoxy}-2-methyl-propionic acid

Base Information

Chemical Name:2-{4-[2-(4-Chloro-benzoylamino)-acetylamino]-phenoxy}-2-methyl-propionic acid
CAS No.:121809-63-0
Molecular Formula:C₁₉H₁₉ClN₂O₅
Molecular Weight:390.823
Hs Code.:

Synonyms:2-{4-[2-(4-Chloro-benzoylamino)-acetylamino]-phenoxy}-2-methyl-propionic acid

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Chemical Property of 2-{4-[2-(4-Chloro-benzoylamino)-acetylamino]-phenoxy}-2-methyl-propionic acid

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Technology Process of 2-{4-[2-(4-Chloro-benzoylamino)-acetylamino]-phenoxy}-2-methyl-propionic acid

There total 6 articles about 2-{4-[2-(4-Chloro-benzoylamino)-acetylamino]-phenoxy}-2-methyl-propionic 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: 66.0%

: 117011-70-8
2-(4-aminophenoxy)-2-methyl propionic acid

: 121809-92-5
4-chlorohippuryl chloride

: 121809-63-0
2-{4-[2-(4-Chloro-benzoylamino)-acetylamino]-phenoxy}-2-methyl-propionic acid

Guidance literature:: With sodium hydroxide; In tetrahydrofuran;
DOI:10.1021/jm00130a021

Reference yield:

: 7159-95-7
(4-hydroxyphenyl)carbamic acid ethyl ester

: 121809-63-0
2-{4-[2-(4-Chloro-benzoylamino)-acetylamino]-phenoxy}-2-methyl-propionic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 48 percent / NaOH / 4 h / Heating

2: 87 percent / 10percent KOH / 0.5 h / Heating

3: 66 percent / 2 N NaOH / tetrahydrofuran

With potassium hydroxide; sodium hydroxide; In tetrahydrofuran;
DOI:10.1021/jm00130a021

Reference yield:

: 767-00-0
4-cyanophenol

: 121809-63-0
2-{4-[2-(4-Chloro-benzoylamino)-acetylamino]-phenoxy}-2-methyl-propionic acid

Guidance literature:: Multi-step reaction with 4 steps

1: 78 percent / NaOH / a) 20 min, b) reflux, 4 h

2: 88 percent / 3percent H₂O₂, KOH / H₂O

3: 90 percent / Br₂, NaOH / H₂O / 0.5 h / 75 °C

4: 66 percent / 2 N NaOH / tetrahydrofuran

With potassium hydroxide; sodium hydroxide; dihydrogen peroxide; bromine; In tetrahydrofuran; water;
DOI:10.1021/jm00130a021