(R)-N-[(S)-1-phenylethyl]-2-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-1,2,3,6-tetrahydropyridine

Base Information

Chemical Name:(R)-N-[(S)-1-phenylethyl]-2-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-1,2,3,6-tetrahydropyridine
CAS No.:1350716-17-4
Molecular Formula:C₁₈H₂₅NO₂
Molecular Weight:287.402
Hs Code.:

Synonyms:(R)-N-[(S)-1-phenylethyl]-2-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-1,2,3,6-tetrahydropyridine

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Chemical Property of (R)-N-[(S)-1-phenylethyl]-2-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-1,2,3,6-tetrahydropyridine

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Technology Process of (R)-N-[(S)-1-phenylethyl]-2-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-1,2,3,6-tetrahydropyridine

There total 3 articles about (R)-N-[(S)-1-phenylethyl]-2-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-1,2,3,6-tetrahydropyridine 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: 87.0%

: 1350716-16-3
(R)-N-allyl-N-[(S)-1-phenylethyl]-1-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-3-buten-1-amine

: 1350716-17-4
(R)-N-[(S)-1-phenylethyl]-2-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-1,2,3,6-tetrahydropyridine

Guidance literature:: With Grubbs catalyst first generation; In dichloromethane; at 20 ℃; for 12h;
DOI:10.1039/c1ob06216f

Reference yield:

: C₁₄H₁₉NO₂

: 1350716-17-4
(R)-N-[(S)-1-phenylethyl]-2-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-1,2,3,6-tetrahydropyridine

Guidance literature:: Multi-step reaction with 3 steps

1: diethyl ether / 12 h / -20 °C / Inert atmosphere

2: sodium hydrogencarbonate; lithium iodide / acetonitrile / 36 h / Reflux

3: Grubbs catalyst first generation / dichloromethane / 12 h / 20 °C

With Grubbs catalyst first generation; sodium hydrogencarbonate; lithium iodide; In diethyl ether; dichloromethane; acetonitrile;
DOI:10.1039/c1ob06216f

Reference yield:

: 1350716-23-2
(R)-N-[(S)-1-phenylethyl]-1-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-3-buten-1-amine

: 1350716-17-4
(R)-N-[(S)-1-phenylethyl]-2-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-1,2,3,6-tetrahydropyridine

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydrogencarbonate; lithium iodide / acetonitrile / 36 h / Reflux

2: Grubbs catalyst first generation / dichloromethane / 12 h / 20 °C

With Grubbs catalyst first generation; sodium hydrogencarbonate; lithium iodide; In dichloromethane; acetonitrile;
DOI:10.1039/c1ob06216f