1-((2-((trans-4-(tert-butyl)cyclohexyl)oxy)naphthalen-1-yl)methyl)piperidine-4-carboxylic acid

Base Information

Chemical Name:1-((2-((trans-4-(tert-butyl)cyclohexyl)oxy)naphthalen-1-yl)methyl)piperidine-4-carboxylic acid
CAS No.:1621065-24-4
Molecular Formula:C₂₇H₃₇NO₃
Molecular Weight:423.596
Hs Code.:

Synonyms:1-((2-((trans-4-(tert-butyl)cyclohexyl)oxy)naphthalen-1-yl)methyl)piperidine-4-carboxylic acid

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Chemical Property of 1-((2-((trans-4-(tert-butyl)cyclohexyl)oxy)naphthalen-1-yl)methyl)piperidine-4-carboxylic acid

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Technology Process of 1-((2-((trans-4-(tert-butyl)cyclohexyl)oxy)naphthalen-1-yl)methyl)piperidine-4-carboxylic acid

There total 4 articles about 1-((2-((trans-4-(tert-butyl)cyclohexyl)oxy)naphthalen-1-yl)methyl)piperidine-4-carboxylic 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: 6.0%

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

: 102010-74-2
ethyl 1-((2-hydroxynaphthalen-1-yl)methyl)piperidine-4-carboxylate

: 1621065-24-4
1-((2-((trans-4-(tert-butyl)cyclohexyl)oxy)naphthalen-1-yl)methyl)piperidine-4-carboxylic acid

Guidance literature:: methanesulfonic acid 4-tert-butylcyclohexyl ester; ethyl 1-((2-hydroxynaphthalen-1-yl)methyl)piperidine-4-carboxylate; With caesium carbonate; In tert-butyl alcohol; for 6h; Reflux;

With water; sodium hydroxide; In N,N-dimethyl-formamide; at 100 ℃; for 1h;

Reference yield:

: 52805-48-8
2-(Benzyloxy)-1-naphthaldehyde

: 1621065-24-4
1-((2-((trans-4-(tert-butyl)cyclohexyl)oxy)naphthalen-1-yl)methyl)piperidine-4-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: ethanol / 2 h / Reflux

1.2: 16 h / 20 °C

2.1: palladium 10% on activated carbon; hydrogen / ethyl acetate / 16 h / 20 °C

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

3.2: 1 h / 100 °C

With palladium 10% on activated carbon; hydrogen; caesium carbonate; In ethanol; ethyl acetate; tert-butyl alcohol;

Reference yield:

: 708-06-5
2-hydroxynaphthalene-1-carbaldehyde

: 1621065-24-4
1-((2-((trans-4-(tert-butyl)cyclohexyl)oxy)naphthalen-1-yl)methyl)piperidine-4-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / tetrahydrofuran / 2 h / Reflux

2.1: ethanol / 2 h / Reflux

2.2: 16 h / 20 °C

3.1: palladium 10% on activated carbon; hydrogen / ethyl acetate / 16 h / 20 °C

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

4.2: 1 h / 100 °C

With palladium 10% on activated carbon; hydrogen; potassium carbonate; caesium carbonate; In tetrahydrofuran; ethanol; ethyl acetate; tert-butyl alcohol;