p-nitrophenyl (1-diazocyclopenta-2,4-dien-2-ylcarbonyloxy)acetate

Base Information

• Chemical Name: p-nitrophenyl (1-diazocyclopenta-2,4-dien-2-ylcarbonyloxy)acetate
• CAS No.: 366446-41-5
• Molecular Formula: C₁₄H₉N₃O₆
• Molecular Weight: 315.242
• Mol file: 366446-41-5.mol

Synonyms:p-nitrophenyl (1-diazocyclopenta-2,4-dien-2-ylcarbonyloxy)acetate

Chemical Property of p-nitrophenyl (1-diazocyclopenta-2,4-dien-2-ylcarbonyloxy)acetate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of p-nitrophenyl (1-diazocyclopenta-2,4-dien-2-ylcarbonyloxy)acetate

There total 3 articles about p-nitrophenyl (1-diazocyclopenta-2,4-dien-2-ylcarbonyloxy)acetate 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%

Iodoacetic acid 4-nitrophenyl ester (31252-85-4) + diazocyclopentadien-2-ylcarboxylic acid (30778-59-7) → p-nitrophenyl (1-diazocyclopenta-2,4-dien-2-ylcarbonyloxy)acetate (366446-41-5)

Guidance literature:

With triethylamine; In acetone; at 20 ℃;

DOI:10.1039/b104945n

Reference yield:

4-nitro-phenol (100-02-7,78813-13-5,89830-32-0) → p-nitrophenyl (1-diazocyclopenta-2,4-dien-2-ylcarbonyloxy)acetate (366446-41-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 55 percent / DCC / CHCl₃ / 0 - 20 °C

2: 80 percent / Et₃N / acetone

With triethylamine; dicyclohexyl-carbodiimide; In chloroform; acetone;

DOI:10.1023/A:1015025609230

Reference yield:

4-nitro-phenol (100-02-7,78813-13-5,89830-32-0) → p-nitrophenyl (1-diazocyclopenta-2,4-dien-2-ylcarbonyloxy)acetate (366446-41-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 55 percent / DCC / CHCl₃; CCl₄ / 0 - 20 °C

2: 80 percent / Et₃N / acetone / 20 °C

With triethylamine; dicyclohexyl-carbodiimide; In tetrachloromethane; chloroform; acetone;

DOI:10.1039/b104945n

upstream raw materials:

Iodoacetic acid 4-nitrophenyl ester

diazocyclopentadien-2-ylcarboxylic acid

4-nitro-phenol