2-(2-(4-(3,4-dichlorophenyl)piperidin-1-yl)ethyl)isoindoline-1,3-dione

Base Information

Chemical Name:2-(2-(4-(3,4-dichlorophenyl)piperidin-1-yl)ethyl)isoindoline-1,3-dione
CAS No.:1394388-59-0
Molecular Formula:C₂₁H₂₀Cl₂N₂O₂
Molecular Weight:403.308
Hs Code.:

Synonyms:2-(2-(4-(3,4-dichlorophenyl)piperidin-1-yl)ethyl)isoindoline-1,3-dione

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-(2-(4-(3,4-dichlorophenyl)piperidin-1-yl)ethyl)isoindoline-1,3-dione

Chemical Property:

Purity/Quality:

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Technology Process of 2-(2-(4-(3,4-dichlorophenyl)piperidin-1-yl)ethyl)isoindoline-1,3-dione

There total 7 articles about 2-(2-(4-(3,4-dichlorophenyl)piperidin-1-yl)ethyl)isoindoline-1,3-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: 45.0%

: 574-98-1
2-(2-bromoethyl)isoindoline-1,3-dione

: 99329-54-1
4-(3,4-dichlorophenyl)piperidine

: 1394388-59-0
2-(2-(4-(3,4-dichlorophenyl)piperidin-1-yl)ethyl)isoindoline-1,3-dione

Guidance literature:: With sodium carbonate; sodium iodide; In N,N-dimethyl-formamide; at 90 ℃; for 4h;
DOI:10.1016/j.ejmech.2013.12.056

Reference yield:

: 79099-07-3
N-tert-butyloxycarbonylpiperidin-4-one

: 1394388-59-0
2-(2-(4-(3,4-dichlorophenyl)piperidin-1-yl)ethyl)isoindoline-1,3-dione

Guidance literature:: Multi-step reaction with 6 steps

1.1: diisopropylamine; n-butyllithium / tetrahydrofuran; hexane / 0.33 h / -78 °C

1.2: 3 h / 0 °C

2.1: potassium acetate; 1,1'-bis-(diphenylphosphino)ferrocene; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / dichloromethane; 1,4-dioxane / 17 h / 80 °C

3.1: potassium phosphate; tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane; water / 18 h / 85 °C

4.1: palladium on activated charcoal; hydrogen / methanol / 18 h / 20 °C

5.1: trifluoroacetic acid / dichloromethane / 5 h / 0 - 20 °C

6.1: sodium iodide; sodium carbonate / N,N-dimethyl-formamide / 4 h / 90 °C

With 1,1'-bis-(diphenylphosphino)ferrocene; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium phosphate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; n-butyllithium; palladium on activated charcoal; hydrogen; potassium acetate; sodium carbonate; diisopropylamine; trifluoroacetic acid; sodium iodide; In tetrahydrofuran; 1,4-dioxane; methanol; hexane; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2013.12.056

Reference yield:

: 153655-93-7
tert-butyl-4-(3,4-dichlorophenyl)piperidine-1-carboxylate

: 1394388-59-0
2-(2-(4-(3,4-dichlorophenyl)piperidin-1-yl)ethyl)isoindoline-1,3-dione

Guidance literature:: Multi-step reaction with 2 steps

1: trifluoroacetic acid / dichloromethane / 5 h / 0 - 20 °C

2: sodium iodide; sodium carbonate / N,N-dimethyl-formamide / 4 h / 90 °C

With sodium carbonate; trifluoroacetic acid; sodium iodide; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2013.12.056