4,6-di-tert-butyl-2-{N-[2-(N,N-dimethyl)-aminocyclohexyl]salicaldimino}phenol

Base Information

Chemical Name:4,6-di-tert-butyl-2-{N-[2-(N,N-dimethyl)-aminocyclohexyl]salicaldimino}phenol
CAS No.:320778-99-2
Molecular Formula:C₂₃H₄₀N₂O
Molecular Weight:360.583
Hs Code.:

Synonyms:4,6-di-tert-butyl-2-{N-[2-(N,N-dimethyl)-aminocyclohexyl]salicaldimino}phenol

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Chemical Property of 4,6-di-tert-butyl-2-{N-[2-(N,N-dimethyl)-aminocyclohexyl]salicaldimino}phenol

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Technology Process of 4,6-di-tert-butyl-2-{N-[2-(N,N-dimethyl)-aminocyclohexyl]salicaldimino}phenol

There total 5 articles about 4,6-di-tert-butyl-2-{N-[2-(N,N-dimethyl)-aminocyclohexyl]salicaldimino}phenol 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: 97.0%

: 50-00-0,30525-89-4,61233-19-0
formaldehyd

: 2,4-Di-tert-butyl-6-{[(E)-(1R,2R)-2-dimethylamino-cyclohexylimino]-methyl}-phenol

: 320778-99-2
4,6-di-tert-butyl-2-{N-[2-(N,N-dimethyl)-aminocyclohexyl]salicaldimino}phenol

Guidance literature:: With sodium cyanoborohydride; acetic acid; In acetonitrile;
DOI:10.1016/S0040-4039(00)01501-X

Reference yield: 59.0%

: 320778-98-1
(R,R)-para-tert-butyl salicaldimine

: 320778-99-2
4,6-di-tert-butyl-2-{N-[2-(N,N-dimethyl)-aminocyclohexyl]salicaldimino}phenol

Guidance literature:: (R,R)-para-tert-butyl salicaldimine; With sodium tetrahydroborate; In acetonitrile; for 0.5h; Inert atmosphere;

With acetic acid; In acetonitrile; for 16h; Inert atmosphere;
DOI:10.1021/ja3048046

Reference yield:

: 37942-07-7
3,5-di-tert-butyl-2-hydroxybenzaldehyde

: 320778-99-2
4,6-di-tert-butyl-2-{N-[2-(N,N-dimethyl)-aminocyclohexyl]salicaldimino}phenol

Guidance literature:: Multi-step reaction with 2 steps

1: 40 percent / methanol / 20 °C

2: 97 percent / NaBH₃CN; AcOH / acetonitrile

With sodium cyanoborohydride; acetic acid; In methanol; acetonitrile;
DOI:10.1016/S0040-4039(00)01501-X