2-(4-(3-(4-(2-hydroxy-2-methylpropoxy)-3-methylphenyl)pentan-3-yl)-2-methylphenoxy)acetic acid

Base Information

Chemical Name:2-(4-(3-(4-(2-hydroxy-2-methylpropoxy)-3-methylphenyl)pentan-3-yl)-2-methylphenoxy)acetic acid
CAS No.:1416802-70-4
Molecular Formula:C₂₅H₃₄O₅
Molecular Weight:414.542
Hs Code.:

Synonyms:2-(4-(3-(4-(2-hydroxy-2-methylpropoxy)-3-methylphenyl)pentan-3-yl)-2-methylphenoxy)acetic acid

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Chemical Property of 2-(4-(3-(4-(2-hydroxy-2-methylpropoxy)-3-methylphenyl)pentan-3-yl)-2-methylphenoxy)acetic acid

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Technology Process of 2-(4-(3-(4-(2-hydroxy-2-methylpropoxy)-3-methylphenyl)pentan-3-yl)-2-methylphenoxy)acetic acid

There total 3 articles about 2-(4-(3-(4-(2-hydroxy-2-methylpropoxy)-3-methylphenyl)pentan-3-yl)-2-methylphenoxy)acetic acid 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: 58.0%

: 1416802-53-3
2-(4-(3-(4-(2-ethoxy-2-oxoethoxy)-3-methylphenyl)pentan-3-yl)-2-methylphenoxy)acetic acid

: 75-16-1
methylmagnesium bromide

: 1416802-70-4
2-(4-(3-(4-(2-hydroxy-2-methylpropoxy)-3-methylphenyl)pentan-3-yl)-2-methylphenoxy)acetic acid

Guidance literature:: 2-(4-(3-(4-(2-ethoxy-2-oxoethoxy)-3-methylphenyl)pentan-3-yl)-2-methylphenoxy)acetic acid; methylmagnesium bromide; In tetrahydrofuran; diethyl ether; at 0 ℃; for 3h; Inert atmosphere;

With water; ammonium chloride; In tetrahydrofuran; diethyl ether; at 0 - 20 ℃; Inert atmosphere;

Reference yield:

: 55041-27-5
3,3-bis[4-hydroxy-3-methylphenyl]pentane

: 1416802-70-4
2-(4-(3-(4-(2-hydroxy-2-methylpropoxy)-3-methylphenyl)pentan-3-yl)-2-methylphenoxy)acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydride / N,N-dimethyl-formamide; paraffin oil / 2 h / 20 °C / Inert atmosphere

1.2: 16 h / Inert atmosphere

2.1: lithium hydroxide monohydrate / tetrahydrofuran; methanol / 16 h / 20 °C / Inert atmosphere

3.1: tetrahydrofuran; diethyl ether / 3 h / 0 °C / Inert atmosphere

3.2: 0 - 20 °C / Inert atmosphere

With lithium hydroxide monohydrate; sodium hydride; In tetrahydrofuran; methanol; diethyl ether; N,N-dimethyl-formamide; paraffin oil;

Reference yield:

: 1416802-52-2
diethyl 2,2-((pentane-3,3-diylbis(2-methyl-4,1-phenylene))bis(oxy))diacetate

: 1416802-70-4
2-(4-(3-(4-(2-hydroxy-2-methylpropoxy)-3-methylphenyl)pentan-3-yl)-2-methylphenoxy)acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: lithium hydroxide monohydrate / tetrahydrofuran; methanol / 16 h / 20 °C / Inert atmosphere

2.1: tetrahydrofuran; diethyl ether / 3 h / 0 °C / Inert atmosphere

2.2: 0 - 20 °C / Inert atmosphere

With lithium hydroxide monohydrate; In tetrahydrofuran; methanol; diethyl ether;