(2-butyl-5-nitrobenzofuran-3-yl)-[4-(3-[²H₂]-3-(4-methylphenylsulphonyloxy) propoxy) phenyl]-methanone

Base Information

• Chemical Name: (2-butyl-5-nitrobenzofuran-3-yl)-[4-(3-[²H₂]-3-(4-methylphenylsulphonyloxy) propoxy) phenyl]-methanone
• CAS No.: 1542232-31-4
• Molecular Formula: C₂₉H₂₉NO₈S
• Molecular Weight: 553.601

Synonyms:(2-butyl-5-nitrobenzofuran-3-yl)-[4-(3-[²H₂]-3-(4-methylphenylsulphonyloxy) propoxy) phenyl]-methanone

Chemical Property of (2-butyl-5-nitrobenzofuran-3-yl)-[4-(3-[²H₂]-3-(4-methylphenylsulphonyloxy) propoxy) phenyl]-methanone

Chemical Property:

Purity/Quality:

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Technology Process of (2-butyl-5-nitrobenzofuran-3-yl)-[4-(3-[²H₂]-3-(4-methylphenylsulphonyloxy) propoxy) phenyl]-methanone

There total 2 articles about (2-butyl-5-nitrobenzofuran-3-yl)-[4-(3-[²H₂]-3-(4-methylphenylsulphonyloxy) propoxy) phenyl]-methanone 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: 87.0%

(2-butyl-5-nitrobenzofuran-3-yl)-[4-(3-[2H2]-3-hydroxypropoxy)phenyl]-methanone (1542232-30-3) + p-toluenesulfonyl chloride (98-59-9) → (2-butyl-5-nitrobenzofuran-3-yl)-[4-(3-[2H2]-3-(4-methylphenylsulphonyloxy) propoxy) phenyl]-methanone (1542232-31-4)

Guidance literature:

With triethylamine; In dichloromethane; at 0 - 20 ℃; for 44h; Cooling with ice;

DOI:10.1002/jlcr.3090

Reference yield:

3-[4-(2-butyl-5-nitro-benzofuran-3-carbonyl)phenoxy]-propionic acid (1542232-29-0) → (2-butyl-5-nitrobenzofuran-3-yl)-[4-(3-[2H2]-3-(4-methylphenylsulphonyloxy) propoxy) phenyl]-methanone (1542232-31-4)

Guidance literature:

Multi-step reaction with 2 steps

1: [⁽²⁾H]borane - tetrahydrofuran (1/1) / tetrahydrofuran / 5.5 h / Inert atmosphere; Cooling with ice

2: triethylamine / dichloromethane / 44 h / 0 - 20 °C / Cooling with ice

With [⁽²⁾H]borane - tetrahydrofuran (1/1); triethylamine; In tetrahydrofuran; dichloromethane;

DOI:10.1002/jlcr.3090

Reference yield: 66.0%

(2-butyl-5-nitrobenzofuran-3-yl)-[4-(3-[2H2]-3-(4-methylphenylsulphonyloxy) propoxy) phenyl]-methanone (1542232-31-4) + dibutylamine (111-92-2) → (2-butyl-5-nitrobenzofuran-3-yl)-[4-(3-dibutylamino-(3-[2H2]-propoxy))-phenyl]-methanone (1542232-32-5)

Guidance literature:

In ethanol; for 8h; Reflux;

DOI:10.1002/jlcr.3090

upstream raw materials:

(2-butyl-5-nitrobenzofuran-3-yl)-[4-(3-[²H₂]-3-hydroxypropoxy)phenyl]-methanone

p-toluenesulfonyl chloride

3-[4-(2-butyl-5-nitro-benzofuran-3-carbonyl)phenoxy]-propionic acid

Downstream raw materials:

(2-butyl-5-nitrobenzofuran-3-yl)-[4-(3-di-1-[²H₂]-butylamino-(3-[²H₂]-propoxy))-phenyl]-methanone

(2-butyl-5-nitrobenzofuran-3-yl)-[4-(3-dibutylamino-(3-[²H₂]-propoxy))-phenyl]-methanone

(5-amino-2-butyl-benzofuran-3-yl)-[4-(3-dibutylamino-3-[²H₂]-propoxy)-phenyl]-methanone

(5-amino-2-butyl-benzofuran-3-yl)-[4-(3-di-1-[²H₂]-butylamino-3-[²H₂]-propoxy)-phenyl]-methanone

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