ethyl 1-((2-(((trans)-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidine-4-carboxylate

Base Information

Chemical Name:ethyl 1-((2-(((trans)-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidine-4-carboxylate
CAS No.:1621065-23-3
Molecular Formula:C₃₀H₄₃NO₃
Molecular Weight:465.676
Hs Code.:

Synonyms:ethyl 1-((2-(((trans)-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidine-4-carboxylate

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Chemical Property of ethyl 1-((2-(((trans)-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidine-4-carboxylate

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Technology Process of ethyl 1-((2-(((trans)-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidine-4-carboxylate

There total 7 articles about ethyl 1-((2-(((trans)-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidine-4-carboxylate 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: 19.0%

: 1621064-61-6
2-(((trans)-4-(tert-butyl)cyclohexyl)oxy)-4-methyl-1-naphthaldehyde

: piperidine-4-carboxylic acid ethyl ester hydrochloride

: 1621065-23-3
ethyl 1-((2-(((trans)-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidine-4-carboxylate

Guidance literature:: 2-(((trans)-4-(tert-butyl)cyclohexyl)oxy)-4-methyl-1-naphthaldehyde; piperidine-4-carboxylic acid ethyl ester hydrochloride; In ethanol; for 2h; Reflux;

With sodium cyanoborohydride; acetic acid; In ethanol; Reflux;

Reference yield:

: 57404-87-2
3-methoxy-1-methylnaphthalene

: 1621065-23-3
ethyl 1-((2-(((trans)-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidine-4-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: boron trichloride; tetra-(n-butyl)ammonium iodide / dichloromethane / 1 h / -78 - 0 °C / Inert atmosphere

2.1: triphenylphosphine; di-isopropyl azodicarboxylate / toluene / Reflux

3.1: tin(IV) chloride / 1,2-dichloro-ethane / 1 h / 0 °C

3.2: 2 h / 0 - 20 °C

3.3: 1 h

4.1: ethanol / 2 h / Reflux

4.2: Reflux

With di-isopropyl azodicarboxylate; boron trichloride; tin(IV) chloride; tetra-(n-butyl)ammonium iodide; triphenylphosphine; In ethanol; dichloromethane; 1,2-dichloro-ethane; toluene;

Reference yield:

: 26207-06-7
4-methylnaphthalen-2-ol

: 1621065-23-3
ethyl 1-((2-(((trans)-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidine-4-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: caesium carbonate / tert-butyl alcohol; butanone / 80 °C

2.1: tin(IV) chloride / 1,2-dichloro-ethane / 1 h / 0 °C

2.2: 2 h / 0 - 20 °C

2.3: 1 h

3.1: ethanol / 2 h / Reflux

3.2: Reflux

With tin(IV) chloride; caesium carbonate; In ethanol; 1,2-dichloro-ethane; butanone; tert-butyl alcohol;