2,2,5,5-Tetramethyl-2,5-dihydro-1H-pyrrole-3-carboxylic acid {2-[2-(2,4-dichloro-phenoxy)-acetylamino]-ethyl}-amide

Base Information

• Chemical Name: 2,2,5,5-Tetramethyl-2,5-dihydro-1H-pyrrole-3-carboxylic acid {2-[2-(2,4-dichloro-phenoxy)-acetylamino]-ethyl}-amide
• CAS No.: 102131-39-5
• Molecular Formula: C₁₉H₂₅Cl₂N₃O₃
• Molecular Weight: 414.332
• Mol file: 102131-39-5.mol

Synonyms:

Chemical Property of 2,2,5,5-Tetramethyl-2,5-dihydro-1H-pyrrole-3-carboxylic acid {2-[2-(2,4-dichloro-phenoxy)-acetylamino]-ethyl}-amide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2,2,5,5-Tetramethyl-2,5-dihydro-1H-pyrrole-3-carboxylic acid {2-[2-(2,4-dichloro-phenoxy)-acetylamino]-ethyl}-amide

There total 3 articles about 2,2,5,5-Tetramethyl-2,5-dihydro-1H-pyrrole-3-carboxylic acid {2-[2-(2,4-dichloro-phenoxy)-acetylamino]-ethyl}-amide 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:

2,4-Dichlorophenoxyacetic acid (94-75-7,89300-30-1) → 2,2,5,5-Tetramethyl-2,5-dihydro-1H-pyrrole-3-carboxylic acid {2-[2-(2,4-dichloro-phenoxy)-acetylamino]-ethyl}-amide (102131-39-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 98 percent / N,N'-dicyclohexylcarbodiimide / ethyl acetate

2: CHCl₃ / 3 h / Heating

With dicyclohexyl-carbodiimide; In chloroform; ethyl acetate;

DOI:10.1021/jm00157a005

Reference yield:

3,5-Dibromo-4-oxo-2,2,6,6-tetramethylpiperidine Hydrobromide (19971-12-1) → 2,2,5,5-Tetramethyl-2,5-dihydro-1H-pyrrole-3-carboxylic acid {2-[2-(2,4-dichloro-phenoxy)-acetylamino]-ethyl}-amide (102131-39-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 70 percent / H₂O / 3 h / 25 °C

2: CHCl₃ / 3 h / Heating

In chloroform; water;

DOI:10.1021/jm00157a005

Reference yield:

2,2,5,5-Tetramethyl-2,5-dihydro-1H-pyrrole-3-carboxylic acid (2-amino-ethyl)-amide (93799-56-5) + (2,4-Dichloro-phenoxy)-acetic acid 2,5-dioxo-pyrrolidin-1-yl ester (93799-60-1) → 2,2,5,5-Tetramethyl-2,5-dihydro-1H-pyrrole-3-carboxylic acid {2-[2-(2,4-dichloro-phenoxy)-acetylamino]-ethyl}-amide (102131-39-5)

Guidance literature:

In chloroform; for 3h; Heating;

DOI:10.1021/jm00157a005

upstream raw materials:

2,2,5,5-Tetramethyl-2,5-dihydro-1H-pyrrole-3-carboxylic acid (2-amino-ethyl)-amide

(2,4-Dichloro-phenoxy)-acetic acid 2,5-dioxo-pyrrolidin-1-yl ester

2,4-Dichlorophenoxyacetic acid

3,5-Dibromo-4-oxo-2,2,6,6-tetramethylpiperidine Hydrobromide