5-Benzyl-4,6-dioxo-octahydropyrrolo[3,4-b]pyrrole

Base Information

Chemical Name:5-Benzyl-4,6-dioxo-octahydropyrrolo[3,4-b]pyrrole
CAS No.:128740-11-4
Molecular Formula:C13H14N2O2
Molecular Weight:230.266
Hs Code.:
DSSTox Substance ID:DTXSID901169799

Synonyms:128740-11-4;5-Benzyl-4,6-dioxo-octahydropyrrolo[3,4-b]pyrrole;SCHEMBL6214056;ZTLZBZDAOBSZBH-UHFFFAOYSA-N;DTXSID901169799;Tetrahydro-5-(phenylmethyl)pyrrolo[3,4-b]pyrrole-4,6(1H,5H)-dione

Suppliers and Price of 5-Benzyl-4,6-dioxo-octahydropyrrolo[3,4-b]pyrrole

Supply Marketing:

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

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Chemical Property of 5-Benzyl-4,6-dioxo-octahydropyrrolo[3,4-b]pyrrole

Chemical Property:

XLogP3:0.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:230.105527694
Heavy Atom Count:17
Complexity:336

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CNC2C1C(=O)N(C2=O)CC3=CC=CC=C3

Technology Process of 5-Benzyl-4,6-dioxo-octahydropyrrolo[3,4-b]pyrrole

There total 3 articles about 5-Benzyl-4,6-dioxo-octahydropyrrolo[3,4-b]pyrrole 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: 56.0%

: 1-benzyl-3-[(2-chloroethyl)amino]pyrrolidine-2,5-dione

: 128740-11-4
5-benzyl-octahydropyrrolo [3,4-b]pyrrole-4,6-dione

Guidance literature:: In N-methyl-acetamide;

Reference yield:

: 1631-26-1
1-benzyl-1H-pyrrole-2,5-dione

: 128740-11-4
5-benzyl-octahydropyrrolo [3,4-b]pyrrole-4,6-dione

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / 1,4-dioxane / Reflux

2: dichloromethane / 48 h / 20 °C

3: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1 h / 0 - 20 °C

4: trifluoroacetic acid / dichloromethane / 1 h / 20 °C

With sodium hydride; triethylamine; trifluoroacetic acid; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: tert-butyl N-(1-benzyl-2,5-dioxopyrrolidin-3-yl)-N-(2-chloroethyl)carbamate

: 128740-11-4
5-benzyl-octahydropyrrolo [3,4-b]pyrrole-4,6-dione

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1 h / 0 - 20 °C

2: trifluoroacetic acid / dichloromethane / 1 h / 20 °C

With sodium hydride; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide; mineral oil;