bis(8-hydroxyoctyl) N-tert-butoxycarbonyl-5-aminoisophthalate

Base Information

• Chemical Name: bis(8-hydroxyoctyl) N-tert-butoxycarbonyl-5-aminoisophthalate
• CAS No.: 406206-23-3
• Molecular Formula: C₂₉H₄₇NO₈
• Molecular Weight: 537.694
• Mol file: 406206-23-3.mol

Synonyms:bis(8-hydroxyoctyl) N-tert-butoxycarbonyl-5-aminoisophthalate

Chemical Property of bis(8-hydroxyoctyl) N-tert-butoxycarbonyl-5-aminoisophthalate

Chemical Property:

Purity/Quality:

Safty Information:

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MSDS Files:

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Technology Process of bis(8-hydroxyoctyl) N-tert-butoxycarbonyl-5-aminoisophthalate

There total 5 articles about bis(8-hydroxyoctyl) N-tert-butoxycarbonyl-5-aminoisophthalate 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: 70.0%

bis[8-[(tetrahydro-2H-pyran-2-yl)oxy]octyl] N-tert-butoxycarbonyl-5-aminoisophthalate (406206-22-2) → bis(8-hydroxyoctyl) N-tert-butoxycarbonyl-5-aminoisophthalate (406206-23-3)

Guidance literature:

With hydrogenchloride; In methanol; at 20 ℃; for 1h;

DOI:10.1021/jo0160930

Reference yield:

8-(tetrahydro-2H-pyran-2-yloxy)octan-1-ol (51326-52-4) → bis(8-hydroxyoctyl) N-tert-butoxycarbonyl-5-aminoisophthalate (406206-23-3)

Guidance literature:

Multi-step reaction with 4 steps

1: 82 percent / triethylamine / tetrahydrofuran / 2 h / 0 °C

2: hydrogen; HCl / PtO₂ / aq. ethanol / 2 h / 1292.9 Torr

3: tetrahydrofuran / 16 h / 20 °C

4: 70 percent / aq. HCl / methanol / 1 h / 20 °C

With hydrogenchloride; hydrogen; triethylamine; platinum(IV) oxide; In tetrahydrofuran; methanol; ethanol;

DOI:10.1021/jo0160930

Reference yield:

5-nitro-1,3-benzenedicarbonylchloride (13438-30-7) → bis(8-hydroxyoctyl) N-tert-butoxycarbonyl-5-aminoisophthalate (406206-23-3)

Guidance literature:

Multi-step reaction with 4 steps

1: 82 percent / triethylamine / tetrahydrofuran / 2 h / 0 °C

2: hydrogen; HCl / PtO₂ / aq. ethanol / 2 h / 1292.9 Torr

3: tetrahydrofuran / 16 h / 20 °C

4: 70 percent / aq. HCl / methanol / 1 h / 20 °C

With hydrogenchloride; hydrogen; triethylamine; platinum(IV) oxide; In tetrahydrofuran; methanol; ethanol;

DOI:10.1021/jo0160930

upstream raw materials:

bis[8-[(tetrahydro-2H-pyran-2-yl)oxy]octyl] N-tert-butoxycarbonyl-5-aminoisophthalate

8-(tetrahydro-2H-pyran-2-yloxy)octan-1-ol

5-nitro-1,3-benzenedicarbonylchloride

bis[8-[(tetrahydro-2H-pyran-2-yl)oxy]octyl] 5-nitroisophthalate