1-{4-[(1-cyclobutylpiperidin-4-ylidene)methyl]phenyl}-4-(methoxymethyl)cyclohexanol

Base Information

Chemical Name:1-{4-[(1-cyclobutylpiperidin-4-ylidene)methyl]phenyl}-4-(methoxymethyl)cyclohexanol
CAS No.:1425971-65-8
Molecular Formula:C₂₄H₃₅NO₂
Molecular Weight:369.547
Hs Code.:

Synonyms:1-{4-[(1-cyclobutylpiperidin-4-ylidene)methyl]phenyl}-4-(methoxymethyl)cyclohexanol

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Chemical Property of 1-{4-[(1-cyclobutylpiperidin-4-ylidene)methyl]phenyl}-4-(methoxymethyl)cyclohexanol

Chemical Property:

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Technology Process of 1-{4-[(1-cyclobutylpiperidin-4-ylidene)methyl]phenyl}-4-(methoxymethyl)cyclohexanol

There total 6 articles about 1-{4-[(1-cyclobutylpiperidin-4-ylidene)methyl]phenyl}-4-(methoxymethyl)cyclohexanol 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:

: 17159-84-1
4-(methoxymethyl)cyclohexan-1-one

: 1425970-11-1
4-(4-bromobenzylidene)-1-cyclobutylpiperidine

: 1425971-64-7
1-{4-[(1-cyclobutylpiperidin-4-ylidene)methyl]phenyl}-4-(methoxymethyl)cyclohexanol

: 1425971-65-8
1-{4-[(1-cyclobutylpiperidin-4-ylidene)methyl]phenyl}-4-(methoxymethyl)cyclohexanol

Guidance literature:: 4-(4-bromobenzylidene)-1-cyclobutylpiperidine; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 0.166667h;

4-(methoxymethyl)cyclohexan-1-one; In tetrahydrofuran; hexane; at 20 ℃; for 3h;

Reference yield:

: 589-15-1
1-bromomethyl-4-bromobenzene

: 1425971-64-7
1-{4-[(1-cyclobutylpiperidin-4-ylidene)methyl]phenyl}-4-(methoxymethyl)cyclohexanol

: 1425971-65-8
1-{4-[(1-cyclobutylpiperidin-4-ylidene)methyl]phenyl}-4-(methoxymethyl)cyclohexanol

Guidance literature:: Multi-step reaction with 5 steps

1.1: toluene / 17 h / 120 °C / Inert atmosphere

2.1: 18-crown-6 ether; potassium carbonate / dichloromethane / 34 h / 45 °C / Inert atmosphere

3.1: hydrogenchloride / 1,4-dioxane / 4 h / 20 °C / Inert atmosphere

4.1: sodium tris(acetoxy)borohydride; acetic acid; triethylamine / dichloromethane / 4.5 h / 20 °C / Inert atmosphere

5.1: n-butyllithium / tetrahydrofuran; hexane / 0.17 h / -78 °C

5.2: 3 h / 20 °C

With hydrogenchloride; n-butyllithium; 18-crown-6 ether; sodium tris(acetoxy)borohydride; potassium carbonate; acetic acid; triethylamine; In tetrahydrofuran; 1,4-dioxane; hexane; dichloromethane; toluene;

Reference yield:

: 4-(4-bromobenzylidene)piperidine hydrochloride

: 1425971-64-7
1-{4-[(1-cyclobutylpiperidin-4-ylidene)methyl]phenyl}-4-(methoxymethyl)cyclohexanol

: 1425971-65-8
1-{4-[(1-cyclobutylpiperidin-4-ylidene)methyl]phenyl}-4-(methoxymethyl)cyclohexanol

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium tris(acetoxy)borohydride; acetic acid; triethylamine / dichloromethane / 4.5 h / 20 °C / Inert atmosphere

2.1: n-butyllithium / tetrahydrofuran; hexane / 0.17 h / -78 °C

2.2: 3 h / 20 °C

With n-butyllithium; sodium tris(acetoxy)borohydride; acetic acid; triethylamine; In tetrahydrofuran; hexane; dichloromethane;