2-Oxopyrrolidine-1-carbonyl chloride

Base Information

• Chemical Name: 2-Oxopyrrolidine-1-carbonyl chloride
• CAS No.: 41341-01-9
• Molecular Formula: C5H6ClNO2
• Molecular Weight: 147.561
• Hs Code.: 2933790090
• European Community (EC) Number: 823-995-0
• DSSTox Substance ID: DTXSID80602061
• Wikidata: Q82499000
• Mol file: 41341-01-9.mol

Synonyms:2-oxopyrrolidine-1-carbonyl chloride;41341-01-9;1-Pyrrolidinecarbonyl chloride, 2-oxo- (9CI);2-Oxo-1-pyrrolidinecarbonyl chloride;1-PYRROLIDINECARBONYL CHLORIDE, 2-OXO-;N-chloroformylbutyrolactam;SCHEMBL3404151;DTXSID80602061;UMLPONXXJIKBMA-UHFFFAOYSA-N;2-Oxo-1-pyrrolidinecarbonylchloride;DB-268744;G47127;EN300-1721415

Chemical Property of 2-Oxopyrrolidine-1-carbonyl chloride

Chemical Property:

• PSA: 37.38000
• LogP: 0.90550
• XLogP3: 1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 147.0087061
• Heavy Atom Count: 9
• Complexity: 157

Purity/Quality:

99% ^*data from raw suppliers

2-Oxopyrrolidine-1-carbonylchloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CC(=O)N(C1)C(=O)Cl

Technology Process of 2-Oxopyrrolidine-1-carbonyl chloride

There total 2 articles about 2-Oxopyrrolidine-1-carbonyl chloride 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: 100.0%

2-pyrrolidinon (616-45-5) + bis(trichloromethyl) carbonate (32315-10-9) → 2-oxopyrrolidin-1-formyl chloride (41341-01-9)

Guidance literature:

With triethylamine; In dichloromethane; at -10 - 20 ℃; for 4h;

Reference yield: 72.0%

2-pyrrolidinon (616-45-5) + phosgene (75-44-5) → 2-oxopyrrolidin-1-formyl chloride (41341-01-9)

Guidance literature:

With triethylamine; In toluene; at 0 - 20 ℃;

Reference yield: 17.0%

icaritin (118525-40-9) + 2-oxopyrrolidin-1-formyl chloride (41341-01-9) → C31H30N2O10

Guidance literature:

With pyridine; In dichloromethane; at 20 ℃; Inert atmosphere;

upstream raw materials:

2-pyrrolidinon

phosgene

bis(trichloromethyl) carbonate

Downstream raw materials:

2-{[(5E)-2-(1,2-diazinan-1-yl)-4-oxo-4,5-dihydro-1,3-thiazol-5-ylidene]methyl}-5-fluorophenyl 2-oxopyrrolidine-1-carboxylate

2-{[(5E)-2-(1,2-diazinan-1-yl)-4-oxo-4,5-dihydro-1,3-thiazol-5-ylidene]methyl}-5-fluorophenyl 5-chloro-2,3-dihydro-1H-pyrrole-1-carboxylate

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