5'-bromo-1-(4-methoxybenzyl)-3-methyl-1',3'-dihydro-2H,5H-spiro[imidazolidine-4,2'-indene]-2,5-dione

Base Information

Chemical Name:5'-bromo-1-(4-methoxybenzyl)-3-methyl-1',3'-dihydro-2H,5H-spiro[imidazolidine-4,2'-indene]-2,5-dione
CAS No.:1210815-86-3
Molecular Formula:C₂₀H₁₉BrN₂O₃
Molecular Weight:415.286
Hs Code.:

Synonyms:5'-bromo-1-(4-methoxybenzyl)-3-methyl-1',3'-dihydro-2H,5H-spiro[imidazolidine-4,2'-indene]-2,5-dione

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Chemical Property of 5'-bromo-1-(4-methoxybenzyl)-3-methyl-1',3'-dihydro-2H,5H-spiro[imidazolidine-4,2'-indene]-2,5-dione

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Technology Process of 5'-bromo-1-(4-methoxybenzyl)-3-methyl-1',3'-dihydro-2H,5H-spiro[imidazolidine-4,2'-indene]-2,5-dione

There total 4 articles about 5'-bromo-1-(4-methoxybenzyl)-3-methyl-1',3'-dihydro-2H,5H-spiro[imidazolidine-4,2'-indene]-2,5-dione 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:

: 1210815-85-2
5'-bromo-1-(4-methoxybenzyl)-1',3'-dihydro-2H,5H-spiro[imidazolidine-4,2'-indene]-2,5-dione

: 74-88-4
methyl iodide

: 1210815-86-3
5'-bromo-1-(4-methoxybenzyl)-3-methyl-1',3'-dihydro-2H,5H-spiro[imidazolidine-4,2'-indene]-2,5-dione

Guidance literature:: 5'-bromo-1-(4-methoxybenzyl)-1',3'-dihydro-2H,5H-spiro[imidazolidine-4,2'-indene]-2,5-dione; With sodium hydride; In N,N-dimethyl-formamide; at -10 - 20 ℃;

methyl iodide; In N,N-dimethyl-formamide; at -10 ℃;

Reference yield:

: 27473-61-6
(+/-)spiro[imidazolidine-4,2'-indane]-2,5-dione

: 1210815-86-3
5'-bromo-1-(4-methoxybenzyl)-3-methyl-1',3'-dihydro-2H,5H-spiro[imidazolidine-4,2'-indene]-2,5-dione

Guidance literature:: Multi-step reaction with 3 steps

1.1: bromine; hydrogen bromide / water / 48 h / 20 °C

2.1: potassium carbonate / N,N-dimethyl-formamide / 18 h / 0 - 20 °C

3.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1 h / -10 - 20 °C

3.2: 1 h / -10 °C

With hydrogen bromide; bromine; sodium hydride; potassium carbonate; In water; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 33584-72-4
5'-bromo-1',3'-dihydro-2H,5H-spiro[imidazolidine-4,2'-indene]-2,5-dione

: 1210815-86-3
5'-bromo-1-(4-methoxybenzyl)-3-methyl-1',3'-dihydro-2H,5H-spiro[imidazolidine-4,2'-indene]-2,5-dione

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 18 h / 0 - 20 °C

2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1 h / -10 - 20 °C

2.2: 1 h / -10 °C

With sodium hydride; potassium carbonate; In N,N-dimethyl-formamide; mineral oil;