5-((-2-((tert-butyloxy)carbonyl)amino)ethoxy)benzene-1,3-dicarboxylic acid

Base Information

• Chemical Name: 5-((-2-((tert-butyloxy)carbonyl)amino)ethoxy)benzene-1,3-dicarboxylic acid
• CAS No.: 198700-44-6
• Molecular Formula: C₁₅H₁₉NO₇
• Molecular Weight: 325.318
• Mol file: 198700-44-6.mol

Synonyms:5-((-2-((tert-butyloxy)carbonyl)amino)ethoxy)benzene-1,3-dicarboxylic acid

Chemical Property of 5-((-2-((tert-butyloxy)carbonyl)amino)ethoxy)benzene-1,3-dicarboxylic acid

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 5-((-2-((tert-butyloxy)carbonyl)amino)ethoxy)benzene-1,3-dicarboxylic acid

There total 6 articles about 5-((-2-((tert-butyloxy)carbonyl)amino)ethoxy)benzene-1,3-dicarboxylic 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: 96.0%

dimethyl 5-((-2-((tert-butyloxy)carbonyl)amino)ethoxy)benzene-1,3-dicarboxylate (198700-45-7) → 5-((-2-((tert-butyloxy)carbonyl)amino)ethoxy)benzene-1,3-dicarboxylic acid (198700-44-6)

Guidance literature:

With lithium hydroxide; In tetrahydrofuran; methanol; water; for 24h;

Reference yield:

Dimethyl 5-hydroxyisophthalate (13036-02-7) → 5-((-2-((tert-butyloxy)carbonyl)amino)ethoxy)benzene-1,3-dicarboxylic acid (198700-44-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 80 percent / NaI; Cs₂CO₃ / butan-2-one / 8 h / 70 °C

2: 77 percent / LiOH / tetrahydrofuran; methanol; H₂O / 1.5 h / 25 °C

With lithium hydroxide; caesium carbonate; sodium iodide; In tetrahydrofuran; methanol; water; butanone; 1: Substitution / 2: Hydrolysis;

DOI:10.1016/S0968-0896(98)00128-X

Reference yield:

2-(tert-butoxycarbonylamino)ethyl bromide (39684-80-5) → 5-((-2-((tert-butyloxy)carbonyl)amino)ethoxy)benzene-1,3-dicarboxylic acid (198700-44-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 80 percent / NaI; Cs₂CO₃ / butan-2-one / 8 h / 70 °C

2: 77 percent / LiOH / tetrahydrofuran; methanol; H₂O / 1.5 h / 25 °C

With lithium hydroxide; caesium carbonate; sodium iodide; In tetrahydrofuran; methanol; water; butanone; 1: Substitution / 2: Hydrolysis;

DOI:10.1016/S0968-0896(98)00128-X

upstream raw materials:

dimethyl 5-((-2-((tert-butyloxy)carbonyl)amino)ethoxy)benzene-1,3-dicarboxylate

2-(tert-butoxycarbonylamino)ethyl bromide

Dimethyl 5-hydroxyisophthalate

5-(2-phthalimidoethoxy)-isophthalic acid dimethyl ester

Downstream raw materials:

C₆₃H₇₅F₂N₇O₁₃

α-[5-(2-t-butoxycarbamylethoxy)-(3,5-biscarbonylphenyl)]-ω-(tetra-oxymethyl)-poly[iminoethoxy-(3,5-bis(carbonylphenyl))]