3-(benzyloxymethyl)-N-(tert-butoxycarbonyl)-3-(11-hydroxyundecyl)piperidine

Base Information

Chemical Name:3-(benzyloxymethyl)-N-(tert-butoxycarbonyl)-3-(11-hydroxyundecyl)piperidine
CAS No.:1392109-81-7
Molecular Formula:C₂₉H₄₉NO₄
Molecular Weight:475.712
Hs Code.:

Synonyms:3-(benzyloxymethyl)-N-(tert-butoxycarbonyl)-3-(11-hydroxyundecyl)piperidine

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Chemical Property of 3-(benzyloxymethyl)-N-(tert-butoxycarbonyl)-3-(11-hydroxyundecyl)piperidine

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Technology Process of 3-(benzyloxymethyl)-N-(tert-butoxycarbonyl)-3-(11-hydroxyundecyl)piperidine

There total 8 articles about 3-(benzyloxymethyl)-N-(tert-butoxycarbonyl)-3-(11-hydroxyundecyl)piperidine 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:

: 1392109-79-3
3-(benzyloxymethyl)-N-(tert-butoxycarbonyl)-3-[(11-tertbutyldiphenylsilyloxy)undecyl]piperidine

: 1392109-81-7
3-(benzyloxymethyl)-N-(tert-butoxycarbonyl)-3-(11-hydroxyundecyl)piperidine

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; Inert atmosphere;
DOI:10.1021/ol301672y

Reference yield:

: 675-20-7
piperidin-2-one

: 1392109-81-7
3-(benzyloxymethyl)-N-(tert-butoxycarbonyl)-3-(11-hydroxyundecyl)piperidine

Guidance literature:: Multi-step reaction with 8 steps

1.1: n-butyllithium / tetrahydrofuran / 0.25 h / -78 °C / Inert atmosphere

1.2: 0.5 h / -78 °C / Inert atmosphere

2.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / -78 °C

2.2: 2 h

3.1: sodium hydride / N,N-dimethyl-formamide / 0.33 h / 0 °C / Inert atmosphere

3.2: 80 °C / Inert atmosphere

4.1: trifluoroacetic acid / dichloromethane / 1 h / 20 °C

5.1: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / Inert atmosphere; Reflux

6.1: dichloromethane / 2 h / 20 °C / Inert atmosphere

7.1: tetra-(n-butyl)ammonium iodide; sodium hydride / tetrahydrofuran / 20 h / Inert atmosphere; Reflux

8.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 20 °C / Inert atmosphere

With lithium aluminium tetrahydride; n-butyllithium; tetrabutyl ammonium fluoride; tetra-(n-butyl)ammonium iodide; sodium hydride; trifluoroacetic acid; lithium hexamethyldisilazane; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ol301672y

Reference yield:

: 1392109-78-2
N-(tert-butoxycarbonyl)-3-[(11-tert-butyldiphenylsilyloxy)undecyl]-3-(hydroxymethyl)piperidine

: 1392109-81-7
3-(benzyloxymethyl)-N-(tert-butoxycarbonyl)-3-(11-hydroxyundecyl)piperidine

Guidance literature:: Multi-step reaction with 2 steps

1: tetra-(n-butyl)ammonium iodide; sodium hydride / tetrahydrofuran / 20 h / Inert atmosphere; Reflux

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 20 °C / Inert atmosphere

With tetrabutyl ammonium fluoride; tetra-(n-butyl)ammonium iodide; sodium hydride; In tetrahydrofuran;
DOI:10.1021/ol301672y