((4S,5S)-5-{[Bis-(4-methyl-benzyl)-amino]-methyl}-2,2-dipropyl-[1,3]dioxolan-4-ylmethyl)-bis-(4-methyl-benzyl)-amine

Base Information

Chemical Name:((4S,5S)-5-{[Bis-(4-methyl-benzyl)-amino]-methyl}-2,2-dipropyl-[1,3]dioxolan-4-ylmethyl)-bis-(4-methyl-benzyl)-amine
CAS No.:515871-46-2
Molecular Formula:C₄₃H₅₆N₂O₂
Molecular Weight:632.93
Hs Code.:

Synonyms:((4S,5S)-5-{[Bis-(4-methyl-benzyl)-amino]-methyl}-2,2-dipropyl-[1,3]dioxolan-4-ylmethyl)-bis-(4-methyl-benzyl)-amine

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Chemical Property of ((4S,5S)-5-{[Bis-(4-methyl-benzyl)-amino]-methyl}-2,2-dipropyl-[1,3]dioxolan-4-ylmethyl)-bis-(4-methyl-benzyl)-amine

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Technology Process of ((4S,5S)-5-{[Bis-(4-methyl-benzyl)-amino]-methyl}-2,2-dipropyl-[1,3]dioxolan-4-ylmethyl)-bis-(4-methyl-benzyl)-amine

There total 5 articles about ((4S,5S)-5-{[Bis-(4-methyl-benzyl)-amino]-methyl}-2,2-dipropyl-[1,3]dioxolan-4-ylmethyl)-bis-(4-methyl-benzyl)-amine 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: 69.0%

: 104-82-5
4-Methylbenzyl chloride

: C-((4S,5S)-5-Aminomethyl-2,2-dipropyl-[1,3]dioxolan-4-yl)-methylamine

: 515871-46-2
((4S,5S)-5-{[Bis-(4-methyl-benzyl)-amino]-methyl}-2,2-dipropyl-[1,3]dioxolan-4-ylmethyl)-bis-(4-methyl-benzyl)-amine

Guidance literature:: With tetra-(n-butyl)ammonium iodide; N-ethyl-N,N-diisopropylamine; In acetonitrile; at 20 ℃;
DOI:10.1021/ja037290e

Reference yield:

: 123-19-3
4-heptanone

: 515871-46-2
((4S,5S)-5-{[Bis-(4-methyl-benzyl)-amino]-methyl}-2,2-dipropyl-[1,3]dioxolan-4-ylmethyl)-bis-(4-methyl-benzyl)-amine

Guidance literature:: Multi-step reaction with 4 steps

1.1: TsOH*H₂O / methanol / Heating

2.1: TsOH*H₂O / methanol; toluene / 24 h / Heating

2.2: NH₃ gas / methanol / 2 h / 4 °C

3.1: LiAlH₄ / tetrahydrofuran / 20 h / Heating

4.1: i-Pr₂NEt; tetrabutylammonium iodide / acetonitrile / 0 °C

With lithium aluminium tetrahydride; tetra-(n-butyl)ammonium iodide; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; toluene; acetonitrile;
DOI:10.1016/j.tet.2004.05.120

Reference yield:

: 515870-48-1
(4R,5R)-2,2-Dipropyl-[1,3]dioxolane-4,5-dicarboxylic acid diamide

: 515871-46-2
((4S,5S)-5-{[Bis-(4-methyl-benzyl)-amino]-methyl}-2,2-dipropyl-[1,3]dioxolan-4-ylmethyl)-bis-(4-methyl-benzyl)-amine

Guidance literature:: Multi-step reaction with 2 steps

1: LiAlH₄ / tetrahydrofuran / 20 h / Heating

2: i-Pr₂NEt; tetrabutylammonium iodide / acetonitrile / 0 °C

With lithium aluminium tetrahydride; tetra-(n-butyl)ammonium iodide; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; acetonitrile;
DOI:10.1016/j.tet.2004.05.120