3-(4-Methoxybenzoyl)-1-methylpyrrolidine-2,5-dione

Base Information

• Chemical Name: 3-(4-Methoxybenzoyl)-1-methylpyrrolidine-2,5-dione
• CAS No.: 92001-77-9
• Molecular Formula: C₁₃H₁₃NO₄
• Molecular Weight: 247.251
• DSSTox Substance ID: DTXSID00524276
• Mol file: 92001-77-9.mol

Synonyms:92001-77-9;3-(4-Methoxybenzoyl)-1-methylpyrrolidine-2,5-dione;DTXSID00524276

Chemical Property of 3-(4-Methoxybenzoyl)-1-methylpyrrolidine-2,5-dione

Chemical Property:

• XLogP3: 0.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 247.08445790
• Heavy Atom Count: 18
• Complexity: 371

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CN1C(=O)CC(C1=O)C(=O)C2=CC=C(C=C2)OC

Technology Process of 3-(4-Methoxybenzoyl)-1-methylpyrrolidine-2,5-dione

There total 1 articles about 3-(4-Methoxybenzoyl)-1-methylpyrrolidine-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: 25.0%

N-methylsuccinimide (1121-07-9) → 3-(4-methoxybenzoyl)-1-methylpyrrolidine-2,5-dione (92001-77-9)

Guidance literature:

With sodium hydride; In tetrahydrofuran; Heating;

Reference yield: 28.0%

Phenylselenyl chloride (5707-04-0) + 3-(4-methoxybenzoyl)-1-methylpyrrolidine-2,5-dione (92001-77-9) → 3-(4-methoxybenzoyl)-1-methyl-3-phenylselenopyrrolidine-2,5-dione

Guidance literature:

With sodium hydride; In tetrahydrofuran; at 20 ℃; for 0.5h;

Reference yield:

3-(4-methoxybenzoyl)-1-methylpyrrolidine-2,5-dione (92001-77-9) → 3-(4-Methoxy-benzoyl)-1-methyl-pyrrole-2,5-dione (1071139-23-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 28 percent / sodium hydride / tetrahydrofuran / 0.5 h / 20 °C

2: m-chloroperoxybenzoic acid / CH₂Cl₂ / 0.25 h / -15 °C

With sodium hydride; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane;

upstream raw materials:

N-methylsuccinimide

Downstream raw materials:

3-(4-Methoxy-benzoyl)-1-methyl-pyrrole-2,5-dione

(1SR,2SR,5RS,6SR)-1-(4-methoxybenzoyl)-2,5,8-trimethyl-7,9-dioxo-8-azabicyclo<4.3.0>non-3-ene

(1R,2R,6S,7S)-2-(4-Methoxy-benzoyl)-4-methyl-4-aza-tricyclo[5.2.1.0^2,6]dec-8-ene-3,5-dione

(1RS,2SR,6RS,7SR)-2-(4-methoxybenzoyl)-4-methyl-3,5-dioxo-4-azatricyclo<5.2.1.0^2,6>dec-8-ene