4-acetoxy-3,5-di-tert-butyl-2-[1-hydroxy-5-methyl-2-(3-methylbutyl)hexyl]phenol

Base Information

Chemical Name:4-acetoxy-3,5-di-tert-butyl-2-[1-hydroxy-5-methyl-2-(3-methylbutyl)hexyl]phenol
CAS No.:157360-66-2
Molecular Formula:C₂₈H₄₈O₄
Molecular Weight:448.687
Hs Code.:

Synonyms:4-acetoxy-3,5-di-tert-butyl-2-[1-hydroxy-5-methyl-2-(3-methylbutyl)hexyl]phenol

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Chemical Property of 4-acetoxy-3,5-di-tert-butyl-2-[1-hydroxy-5-methyl-2-(3-methylbutyl)hexyl]phenol

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Technology Process of 4-acetoxy-3,5-di-tert-butyl-2-[1-hydroxy-5-methyl-2-(3-methylbutyl)hexyl]phenol

There total 5 articles about 4-acetoxy-3,5-di-tert-butyl-2-[1-hydroxy-5-methyl-2-(3-methylbutyl)hexyl]phenol 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: 46.0%

: 157360-78-6
5-bromo-2,8-dimethylnonane

: 157360-29-7
5-acetoxy-4,6-di-tert-butyl-2-hydroxybenzaldehyde

: 157360-66-2
4-acetoxy-3,5-di-tert-butyl-2-[1-hydroxy-5-methyl-2-(3-methylbutyl)hexyl]phenol

Guidance literature:: With lithium; In tetrahydrofuran; for 24h;
DOI:10.1021/jm030062a

Reference yield:

: 489-01-0
2,6-Di-t-butyl-4-methoxyphenol

: 157360-66-2
4-acetoxy-3,5-di-tert-butyl-2-[1-hydroxy-5-methyl-2-(3-methylbutyl)hexyl]phenol

Guidance literature:: Multi-step reaction with 5 steps

1.1: 88 percent / H₂SO₄ / 2 h / 70 °C

2.1: 80 percent / iodotrimethylsilane / CH₂Cl₂ / 48 h / 20 °C

3.1: AcOH; H₂SO₄ / 48 h / 20 °C

3.2: aq. HCl / ethanol / 2 h / Heating

4.1: 19.0 g / (CH₂)6N₄; aq. AcOH / 4 h / Heating

5.1: 46 percent / Li / tetrahydrofuran / 24 h

With trimethylsilyl iodide; (CH₂)6N₄; sulfuric acid; lithium; acetic acid; In tetrahydrofuran; dichloromethane; 5.1: Barbier reaction;
DOI:10.1021/jm030062a

Reference yield:

: 32102-41-3
4-acetoxy-3,5-di-tert-butylphenol

: 157360-66-2
4-acetoxy-3,5-di-tert-butyl-2-[1-hydroxy-5-methyl-2-(3-methylbutyl)hexyl]phenol

Guidance literature:: Multi-step reaction with 3 steps

1.1: AcOH; H₂SO₄ / 48 h / 20 °C

1.2: aq. HCl / ethanol / 2 h / Heating

2.1: 19.0 g / (CH₂)6N₄; aq. AcOH / 4 h / Heating

3.1: 46 percent / Li / tetrahydrofuran / 24 h

With (CH₂)6N₄; sulfuric acid; lithium; acetic acid; In tetrahydrofuran; 3.1: Barbier reaction;
DOI:10.1021/jm030062a