4-[decyl-(4-{4-[decyl-(4-{4-[decyl-(4-nitro-benzoyl)-amino]-benzoylamino}-benzoyl)-amino]-benzoylamino}-benzoyl)-amino]-benzoic acid ethyl ester

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Chemical Name:4-[decyl-(4-{4-[decyl-(4-{4-[decyl-(4-nitro-benzoyl)-amino]-benzoylamino}-benzoyl)-amino]-benzoylamino}-benzoyl)-amino]-benzoic acid ethyl ester
CAS No.:875573-83-4
Molecular Formula:C₇₄H₉₄N₆O₉
Molecular Weight:1211.6
Hs Code.:

Synonyms:4-[decyl-(4-{4-[decyl-(4-{4-[decyl-(4-nitro-benzoyl)-amino]-benzoylamino}-benzoyl)-amino]-benzoylamino}-benzoyl)-amino]-benzoic acid ethyl ester

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Chemical Property of 4-[decyl-(4-{4-[decyl-(4-{4-[decyl-(4-nitro-benzoyl)-amino]-benzoylamino}-benzoyl)-amino]-benzoylamino}-benzoyl)-amino]-benzoic acid ethyl ester

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Technology Process of 4-[decyl-(4-{4-[decyl-(4-{4-[decyl-(4-nitro-benzoyl)-amino]-benzoylamino}-benzoyl)-amino]-benzoylamino}-benzoyl)-amino]-benzoic acid ethyl ester

There total 9 articles about 4-[decyl-(4-{4-[decyl-(4-{4-[decyl-(4-nitro-benzoyl)-amino]-benzoylamino}-benzoyl)-amino]-benzoylamino}-benzoyl)-amino]-benzoic acid ethyl 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: 80.0%

: 875573-79-8
4-[(4-amino-benzoyl)-decyl-amino]-benzoic acid ethyl ester

: 875573-82-3
4-[decyl-(4-{4-[decyl-(4-nitro-benzoyl)-amino]-benzoylamino}-benzoyl)-amino]-benzoic acid

: 875573-83-4
4-[decyl-(4-{4-[decyl-(4-{4-[decyl-(4-nitro-benzoyl)-amino]-benzoylamino}-benzoyl)-amino]-benzoylamino}-benzoyl)-amino]-benzoic acid ethyl ester

Guidance literature:: With chloro(triphenyl)phosphonium chloride; In chloroform; for 2h; Heating;
DOI:10.1016/j.tetlet.2005.11.084

Reference yield:

: 875573-78-7
4-[decyl-(4-nitro-benzoyl)-amino]-benzoic acid ethyl ester

: 875573-83-4
4-[decyl-(4-{4-[decyl-(4-{4-[decyl-(4-nitro-benzoyl)-amino]-benzoylamino}-benzoyl)-amino]-benzoylamino}-benzoyl)-amino]-benzoic acid ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 94 percent / H₂ / Pd/C / ethanol / 2 h / 20 °C

2: 73 percent / Ph₃PCl₂ / CHCl₃ / 3 h / Heating

3: 81 percent / aq. NaOH / ethanol / 0.5 h / 20 °C

4: 80 percent / Ph₃PCl₂ / CHCl₃ / 2 h / Heating

With sodium hydroxide; hydrogen; chloro(triphenyl)phosphonium chloride; palladium on activated charcoal; In ethanol; chloroform;
DOI:10.1016/j.tetlet.2005.11.084

Reference yield:

: 2050-77-3
Iododecane

: 875573-83-4
4-[decyl-(4-{4-[decyl-(4-{4-[decyl-(4-nitro-benzoyl)-amino]-benzoylamino}-benzoyl)-amino]-benzoylamino}-benzoyl)-amino]-benzoic acid ethyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 68 percent / hexamethylphosphoric acid triamide / 2.5 h / 120 °C

2: 100 percent / pyridine / 1.5 h / 20 °C

3: 94 percent / H₂ / Pd/C / ethanol / 2 h / 20 °C

4: 73 percent / Ph₃PCl₂ / CHCl₃ / 3 h / Heating

5: 81 percent / aq. NaOH / ethanol / 0.5 h / 20 °C

6: 80 percent / Ph₃PCl₂ / CHCl₃ / 2 h / Heating

With pyridine; sodium hydroxide; hydrogen; dichlorotriphenyl-λ⁴-phosphane; palladium on activated charcoal; In N,N,N,N,N,N-hexamethylphosphoric triamide; ethanol; chloroform;
DOI:10.1016/j.tetlet.2005.11.084