(3R,4R,5R)-N-benzyl-4-(benzyloxy)-5-((E)-tetradec-2-en-1-yl)tetrahydrofuran-3-amine

Base Information

Chemical Name:(3R,4R,5R)-N-benzyl-4-(benzyloxy)-5-((E)-tetradec-2-en-1-yl)tetrahydrofuran-3-amine
CAS No.:1340476-27-8
Molecular Formula:C₃₂H₄₇NO₂
Molecular Weight:477.731
Hs Code.:

Synonyms:(3R,4R,5R)-N-benzyl-4-(benzyloxy)-5-((E)-tetradec-2-en-1-yl)tetrahydrofuran-3-amine

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Chemical Property of (3R,4R,5R)-N-benzyl-4-(benzyloxy)-5-((E)-tetradec-2-en-1-yl)tetrahydrofuran-3-amine

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Technology Process of (3R,4R,5R)-N-benzyl-4-(benzyloxy)-5-((E)-tetradec-2-en-1-yl)tetrahydrofuran-3-amine

There total 6 articles about (3R,4R,5R)-N-benzyl-4-(benzyloxy)-5-((E)-tetradec-2-en-1-yl)tetrahydrofuran-3-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: 78.0%

: 2437-56-1
1-tridecene

: 1340476-26-7
(3R,4R,5R)-5-allyl-N-benzyl-4-(benzyloxy)tetrahydrofuran-3-amine

: 1340476-27-8
(3R,4R,5R)-N-benzyl-4-(benzyloxy)-5-((E)-tetradec-2-en-1-yl)tetrahydrofuran-3-amine

Guidance literature:: With Grubbs catalyst first generation; In dichloromethane; for 12h; Reflux; Inert atmosphere;
DOI:10.1016/j.tetasy.2011.07.010

Reference yield:

: 1268616-18-7
(2S,3R,4R)-3-(benzyloxy)-4-(methoxymethoxy)hept-6-ene-1,2-diol

: 1340476-27-8
(3R,4R,5R)-N-benzyl-4-(benzyloxy)-5-((E)-tetradec-2-en-1-yl)tetrahydrofuran-3-amine

Guidance literature:: Multi-step reaction with 4 steps

1: dmap / dichloromethane / 12 h / 0 - 20 °C / Inert atmosphere

2: pyridinium p-toluenesulfonate / methanol / 1 h / Reflux; Inert atmosphere

3: 12 h / 150 °C / Inert atmosphere

4: Grubbs catalyst first generation / dichloromethane / 12 h / Reflux; Inert atmosphere

With Grubbs catalyst first generation; dmap; pyridinium p-toluenesulfonate; In methanol; dichloromethane;
DOI:10.1016/j.tetasy.2011.07.010

Reference yield:

: 1268616-25-6
C₁₉H₂₈O₅

: 1340476-27-8
(3R,4R,5R)-N-benzyl-4-(benzyloxy)-5-((E)-tetradec-2-en-1-yl)tetrahydrofuran-3-amine

Guidance literature:: Multi-step reaction with 5 steps

1: pyridinium p-toluenesulfonate / methanol / 12 h / 20 °C / Inert atmosphere

2: dmap / dichloromethane / 12 h / 0 - 20 °C / Inert atmosphere

3: pyridinium p-toluenesulfonate / methanol / 1 h / Reflux; Inert atmosphere

4: 12 h / 150 °C / Inert atmosphere

5: Grubbs catalyst first generation / dichloromethane / 12 h / Reflux; Inert atmosphere

With Grubbs catalyst first generation; dmap; pyridinium p-toluenesulfonate; In methanol; dichloromethane;
DOI:10.1016/j.tetasy.2011.07.010