3-(5-Iodo-pent-1-ynyl)-4-(2-nitro-benzyloxy)-benzoic acid 2-nitro-benzyl ester

Base Information

• Chemical Name: 3-(5-Iodo-pent-1-ynyl)-4-(2-nitro-benzyloxy)-benzoic acid 2-nitro-benzyl ester
• CAS No.: 184166-95-8
• Molecular Formula: C₂₆H₂₁IN₂O₇
• Molecular Weight: 600.366
• Mol file: 184166-95-8.mol

Synonyms:3-(5-Iodo-pent-1-ynyl)-4-(2-nitro-benzyloxy)-benzoic acid 2-nitro-benzyl ester

Chemical Property of 3-(5-Iodo-pent-1-ynyl)-4-(2-nitro-benzyloxy)-benzoic acid 2-nitro-benzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-(5-Iodo-pent-1-ynyl)-4-(2-nitro-benzyloxy)-benzoic acid 2-nitro-benzyl ester

There total 8 articles about 3-(5-Iodo-pent-1-ynyl)-4-(2-nitro-benzyloxy)-benzoic acid 2-nitro-benzyl 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: 79.0%

3-(5-Hydroxy-pent-1-ynyl)-4-(2-nitro-benzyloxy)-benzoic acid 2-nitro-benzyl ester (184166-90-3) → 3-(5-Iodo-pent-1-ynyl)-4-(2-nitro-benzyloxy)-benzoic acid 2-nitro-benzyl ester (184166-95-8)

Guidance literature:

With methyltriphenoxyphosphonium iodide; In dichloromethane; 1.) -78 deg C, 0.5 h, 2.) RT, 20 h;

DOI:10.1016/0968-0896(96)00139-3

Reference yield:

pent-1-yn-5-ol (5390-04-5) → 3-(5-Iodo-pent-1-ynyl)-4-(2-nitro-benzyloxy)-benzoic acid 2-nitro-benzyl ester (184166-95-8)

Guidance literature:

Multi-step reaction with 4 steps

1: 64 percent / imidazole / dimethylformamide / 16 h / Ambient temperature

2: 60 percent / PdCl₂(PPh₃)2, CuI, Et₃N / CH₂Cl₂ / 24 h / Ambient temperature

3: 80 percent / HOAc, TBAF / tetrahydrofuran / 5 h / Ambient temperature

4: 79 percent / (PhO)3P⁽¹⁺⁾*CH₃I^(1-) / CH₂Cl₂ / 1.) -78 deg C, 0.5 h, 2.) RT, 20 h

With 1H-imidazole; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; tetrabutyl ammonium fluoride; methyltriphenoxyphosphonium iodide; acetic acid; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1016/0968-0896(96)00139-3

Reference yield:

tert-butyl-pent-4-ynyloxy-diphenyl-silane (91266-03-4) → 3-(5-Iodo-pent-1-ynyl)-4-(2-nitro-benzyloxy)-benzoic acid 2-nitro-benzyl ester (184166-95-8)

Guidance literature:

Multi-step reaction with 3 steps

1: 60 percent / PdCl₂(PPh₃)2, CuI, Et₃N / CH₂Cl₂ / 24 h / Ambient temperature

2: 80 percent / HOAc, TBAF / tetrahydrofuran / 5 h / Ambient temperature

3: 79 percent / (PhO)3P⁽¹⁺⁾*CH₃I^(1-) / CH₂Cl₂ / 1.) -78 deg C, 0.5 h, 2.) RT, 20 h

With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; tetrabutyl ammonium fluoride; methyltriphenoxyphosphonium iodide; acetic acid; triethylamine; In tetrahydrofuran; dichloromethane;

DOI:10.1016/0968-0896(96)00139-3

upstream raw materials:

3-(5-Hydroxy-pent-1-ynyl)-4-(2-nitro-benzyloxy)-benzoic acid 2-nitro-benzyl ester

pent-1-yn-5-ol

tert-butyl-pent-4-ynyloxy-diphenyl-silane

2-nitrophenylmethyl bromide