2-(1-((2-((trans-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidin-4-yl)acetic acid

Base Information

Chemical Name:2-(1-((2-((trans-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidin-4-yl)acetic acid
CAS No.:1621064-82-1
Molecular Formula:C₂₉H₄₁NO₃
Molecular Weight:451.649
Hs Code.:

Synonyms:2-(1-((2-((trans-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidin-4-yl)acetic acid

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Chemical Property of 2-(1-((2-((trans-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidin-4-yl)acetic acid

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Technology Process of 2-(1-((2-((trans-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidin-4-yl)acetic acid

There total 4 articles about 2-(1-((2-((trans-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidin-4-yl)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: 70.0%

: 1621064-83-2
methyl 2-(1-((2-((trans-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidin-4-yl)acetate

: 1621064-82-1
2-(1-((2-((trans-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidin-4-yl)acetic acid

Guidance literature:: With water; sodium hydroxide; In tetrahydrofuran; at 60 ℃; for 16h;

Reference yield:

: 18508-91-3
methanesulfonic acid 4-tert-butylcyclohexyl ester

: 1621064-82-1
2-(1-((2-((trans-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidin-4-yl)acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: caesium carbonate / tert-butyl alcohol / 6 h / Reflux

2.1: tetramethoxytitanium / tetrahydrofuran / 16 h / 100 °C / Microwave irradiation

2.2: 1 h / 100 °C / Microwave irradiation

3.1: water; sodium hydroxide / tetrahydrofuran / 16 h / 60 °C

With tetramethoxytitanium; water; caesium carbonate; sodium hydroxide; In tetrahydrofuran; tert-butyl alcohol;

Reference yield:

: 2-(cis-4-tert-butylcyclohexyloxy)-4-methyl-1-naphthaldehyde

: 1621064-82-1
2-(1-((2-((trans-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidin-4-yl)acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: tetramethoxytitanium / tetrahydrofuran / 16 h / 100 °C / Microwave irradiation

1.2: 1 h / 100 °C / Microwave irradiation

2.1: water; sodium hydroxide / tetrahydrofuran / 16 h / 60 °C

With tetramethoxytitanium; water; sodium hydroxide; In tetrahydrofuran;