3--1-(ethoxycarbonyl)-5,6,7,8-tetrahydro-1H-azocin-2-one

Base Information

Chemical Name:3--1-(ethoxycarbonyl)-5,6,7,8-tetrahydro-1H-azocin-2-one
CAS No.:129104-28-5
Molecular Formula:C₂₀H₂₆N₂O₅
Molecular Weight:374.437
Hs Code.:

3-<N-Benzyl-N-(ethoxycarbonyl)amino>-1-(ethoxycarbonyl)-5,6,7,8-tetrahydro-1H-azocin-2-one

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Chemical Property of 3--1-(ethoxycarbonyl)-5,6,7,8-tetrahydro-1H-azocin-2-one

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Technology Process of 3--1-(ethoxycarbonyl)-5,6,7,8-tetrahydro-1H-azocin-2-one

There total 3 articles about 3--1-(ethoxycarbonyl)-5,6,7,8-tetrahydro-1H-azocin-2-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:

: 93350-12-0
Azocane-2,3-dione

: 129104-28-5
3--1-(ethoxycarbonyl)-5,6,7,8-tetrahydro-1H-azocin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 65 percent / p-TsOH / benzene / 5 h / Heating

2: 1) PhMgBr, CuI / 1) DME, diethyl ether, room temp., 15 h, 2) 24 h

With copper(l) iodide; toluene-4-sulfonic acid; phenylmagnesium bromide; In benzene;
DOI:10.1021/jo00305a014

Reference yield:

: 100-46-9
benzylamine

: 129104-28-5
3--1-(ethoxycarbonyl)-5,6,7,8-tetrahydro-1H-azocin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 65 percent / p-TsOH / benzene / 5 h / Heating

2: 1) PhMgBr, CuI / 1) DME, diethyl ether, room temp., 15 h, 2) 24 h

With copper(l) iodide; toluene-4-sulfonic acid; phenylmagnesium bromide; In benzene;
DOI:10.1021/jo00305a014

Reference yield:

: 541-41-3
chloroformic acid ethyl ester

: 129104-27-4
3-(N-Benzylimino)tetrahydro-1H,4H-azocin-2-one

: 129104-28-5
3--1-(ethoxycarbonyl)-5,6,7,8-tetrahydro-1H-azocin-2-one

Guidance literature:: With copper(l) iodide; phenylmagnesium bromide; Yield given. Multistep reaction; 1) DME, diethyl ether, room temp., 15 h, 2) 24 h;
DOI:10.1021/jo00305a014