(2R,3S,5S,6S,E)-(+)-1-allyl-2-(2-(benzyloxy)ethyl)-3-methyl-6-(prop-1-enyl)-5-propylpiperidin-4-one

Base Information

Chemical Name:(2R,3S,5S,6S,E)-(+)-1-allyl-2-(2-(benzyloxy)ethyl)-3-methyl-6-(prop-1-enyl)-5-propylpiperidin-4-one
CAS No.:1205539-08-7
Molecular Formula:C₂₄H₃₅NO₂
Molecular Weight:369.547
Hs Code.:

Synonyms:(2R,3S,5S,6S,E)-(+)-1-allyl-2-(2-(benzyloxy)ethyl)-3-methyl-6-(prop-1-enyl)-5-propylpiperidin-4-one

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Chemical Property of (2R,3S,5S,6S,E)-(+)-1-allyl-2-(2-(benzyloxy)ethyl)-3-methyl-6-(prop-1-enyl)-5-propylpiperidin-4-one

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Technology Process of (2R,3S,5S,6S,E)-(+)-1-allyl-2-(2-(benzyloxy)ethyl)-3-methyl-6-(prop-1-enyl)-5-propylpiperidin-4-one

There total 1 articles about (2R,3S,5S,6S,E)-(+)-1-allyl-2-(2-(benzyloxy)ethyl)-3-methyl-6-(prop-1-enyl)-5-propylpiperidin-4-one 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: 72.0%

: 1205539-07-6
(2R,3S,5S,6S,E)-(-)-2-(2-(benzyloxy)ethyl)-3-methyl-6-(prop-1-enyl)-5-propylpiperidin-4-one

: 106-95-6
allyl bromide

: 1205539-08-7
(2R,3S,5S,6S,E)-(+)-1-allyl-2-(2-(benzyloxy)ethyl)-3-methyl-6-(prop-1-enyl)-5-propylpiperidin-4-one

Guidance literature:: With sodium carbonate; In ethanol; at 20 - 70 ℃; Inert atmosphere;
DOI:10.1039/b915796d

Reference yield: 69.0%

: 1205539-08-7
(2R,3S,5S,6S,E)-(+)-1-allyl-2-(2-(benzyloxy)ethyl)-3-methyl-6-(prop-1-enyl)-5-propylpiperidin-4-one

: 1205539-10-1
(3R,4S)-(+)-1-(benzyloxy)-4-methyl-3-(1H-pyrrol-1-yl)nonan-5-one

: 1205539-09-8
(5R,6S,8S,9S)-(+)-5-(2-(benzyloxy)ethyl)-6-methyl-8-propyl-5,6,8,8a-tetrahydroindolizin-7(3H)-one

Guidance literature:: With Grubbs catalyst first generation; In dichloromethane; at 20 ℃; for 8h; Inert atmosphere;
DOI:10.1039/b915796d

Reference yield: 60.0%

: 1205539-08-7
(2R,3S,5S,6S,E)-(+)-1-allyl-2-(2-(benzyloxy)ethyl)-3-methyl-6-(prop-1-enyl)-5-propylpiperidin-4-one

: 1205539-11-2
(5R,6S,8S,9S)-(-)-5-[2-(benzyloxy)ethyl]-6-methyl-8-propylhexahydroindolizin-7(1H)-one

Guidance literature:: (2R,3S,5S,6S,E)-(+)-1-allyl-2-(2-(benzyloxy)ethyl)-3-methyl-6-(prop-1-enyl)-5-propylpiperidin-4-one; With Grubbs catalyst first generation; In dichloromethane; at 20 ℃; for 3h; Inert atmosphere;

With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; for 2h; under 760.051 Torr;
DOI:10.1039/b915796d