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

Base Information

Chemical Name:methyl 2-(1-((2-((trans-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidin-4-yl)acetate
CAS No.:1621064-83-2
Molecular Formula:C₃₀H₄₃NO₃
Molecular Weight:465.676
Hs Code.:

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

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

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

There total 3 articles about methyl 2-(1-((2-((trans-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidin-4-yl)acetate 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: 56.0%

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

: 168986-49-0
4-piperidine acetic acid methyl ester

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

Guidance literature:: 2-(cis-4-tert-butylcyclohexyloxy)-4-methyl-1-naphthaldehyde; 4-piperidine acetic acid methyl ester; With tetramethoxytitanium; In tetrahydrofuran; at 100 ℃; for 16h; Microwave irradiation;

With sodium tris(acetoxy)borohydride; In tetrahydrofuran; at 100 ℃; for 1h; Microwave irradiation;

Reference yield:

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

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

Guidance literature:: Multi-step reaction with 2 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

With tetramethoxytitanium; caesium carbonate; In tetrahydrofuran; tert-butyl alcohol;

Reference yield:

: 79325-54-5
2-Hydroxy-4-methyl-1-naphthaldehyde

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

Guidance literature:: Multi-step reaction with 2 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

With tetramethoxytitanium; caesium carbonate; In tetrahydrofuran; tert-butyl alcohol;