(E)-3-(4-chlorophenyl)-3-(4-hydroxybut-2-enyloxy)-2-(4-nitrobenzyl)-2,3-dihydroisoindol-1-one

Base Information

Chemical Name:(E)-3-(4-chlorophenyl)-3-(4-hydroxybut-2-enyloxy)-2-(4-nitrobenzyl)-2,3-dihydroisoindol-1-one
CAS No.:1202803-44-8
Molecular Formula:C₂₅H₂₁ClN₂O₅
Molecular Weight:464.905
Hs Code.:

Synonyms:(E)-3-(4-chlorophenyl)-3-(4-hydroxybut-2-enyloxy)-2-(4-nitrobenzyl)-2,3-dihydroisoindol-1-one

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Chemical Property of (E)-3-(4-chlorophenyl)-3-(4-hydroxybut-2-enyloxy)-2-(4-nitrobenzyl)-2,3-dihydroisoindol-1-one

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Technology Process of (E)-3-(4-chlorophenyl)-3-(4-hydroxybut-2-enyloxy)-2-(4-nitrobenzyl)-2,3-dihydroisoindol-1-one

There total 5 articles about (E)-3-(4-chlorophenyl)-3-(4-hydroxybut-2-enyloxy)-2-(4-nitrobenzyl)-2,3-dihydroisoindol-1-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: 58.0%

: 878023-10-0
3-chloro-3-(4-chlorophenyl)-2-(4-nitrobenzyl)-2,3-dihydroisoindolin-1-one

: 6117-80-2
1,4-butenediol

: 1202803-44-8
(E)-3-(4-chlorophenyl)-3-(4-hydroxybut-2-enyloxy)-2-(4-nitrobenzyl)-2,3-dihydroisoindol-1-one

Guidance literature:: With potassium carbonate; In tetrahydrofuran; at 20 ℃; for 4h; Inert atmosphere;

Reference yield:

: 18600-42-5
4-nitrobenzylamine hydrochloride

: 1202803-44-8
(E)-3-(4-chlorophenyl)-3-(4-hydroxybut-2-enyloxy)-2-(4-nitrobenzyl)-2,3-dihydroisoindol-1-one

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / tetrahydrofuran / 4 h / 20 °C / Inert atmosphere

2: thionyl chloride / N,N-dimethyl-formamide / tetrahydrofuran

3: potassium carbonate / tetrahydrofuran / 4 h / 20 °C / Inert atmosphere

With thionyl chloride; potassium carbonate; triethylamine; N,N-dimethyl-formamide; In tetrahydrofuran;

Reference yield:

: 85-56-3
2-(4-chlorobenzoyl)benzoic acid

: 1202803-44-8
(E)-3-(4-chlorophenyl)-3-(4-hydroxybut-2-enyloxy)-2-(4-nitrobenzyl)-2,3-dihydroisoindol-1-one

Guidance literature:: Multi-step reaction with 4 steps

1: thionyl chloride / N,N-dimethyl-formamide / tetrahydrofuran / 4 h / 20 °C / Inert atmosphere

2: triethylamine / tetrahydrofuran / 4 h / 20 °C / Inert atmosphere

3: thionyl chloride / N,N-dimethyl-formamide / tetrahydrofuran

4: potassium carbonate / tetrahydrofuran / 4 h / 20 °C / Inert atmosphere

With thionyl chloride; potassium carbonate; triethylamine; N,N-dimethyl-formamide; In tetrahydrofuran;