N-(1-benzylpiperidin-4-yl)-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-2-carboxamide

Base Information

Chemical Name:N-(1-benzylpiperidin-4-yl)-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-2-carboxamide
CAS No.:1271911-12-6
Molecular Formula:C₂₇H₃₆N₂O
Molecular Weight:404.596
Hs Code.:

Synonyms:N-(1-benzylpiperidin-4-yl)-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-2-carboxamide

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Chemical Property of N-(1-benzylpiperidin-4-yl)-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-2-carboxamide

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Technology Process of N-(1-benzylpiperidin-4-yl)-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-2-carboxamide

There total 5 articles about N-(1-benzylpiperidin-4-yl)-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-2-carboxamide 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:

: 50541-93-0
4-amino-1-benzylpiperidine

: C₁₈H₂₂N₂O

: 1271911-12-6
N-(1-benzylpiperidin-4-yl)-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-2-carboxamide

Guidance literature:: In N,N-dimethyl-formamide; at 20 ℃; Cooling with ice;
DOI:10.1016/j.ejmech.2010.11.021

Reference yield:

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 1271911-12-6
N-(1-benzylpiperidin-4-yl)-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-2-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1: hydrogenchloride / ethanol

2: aluminum (III) chloride

3: potassium permanganate / Alkaline conditions

4: N,N-dimethyl-formamide / 3.5 h / 0 - 20 °C

5: N,N-dimethyl-formamide / 20 °C / Cooling with ice

With hydrogenchloride; aluminum (III) chloride; potassium permanganate; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2010.11.021

Reference yield:

: 6223-78-5
2,5-dichloro-2,5-dimethyl hexane

: 1271911-12-6
N-(1-benzylpiperidin-4-yl)-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-2-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: aluminum (III) chloride

2: potassium permanganate / Alkaline conditions

3: N,N-dimethyl-formamide / 3.5 h / 0 - 20 °C

4: N,N-dimethyl-formamide / 20 °C / Cooling with ice

With aluminum (III) chloride; potassium permanganate; In N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2010.11.021