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Pyrrolidine, 1-[(hexahydro-1,3-dioxo-2-phenyl-1H-pyrrolo[1,2-c]imidazol-5-yl)carbon yl]-

Base Information
  • Chemical Name:Pyrrolidine, 1-[(hexahydro-1,3-dioxo-2-phenyl-1H-pyrrolo[1,2-c]imidazol-5-yl)carbon yl]-
  • CAS No.:90513-81-8
  • Molecular Formula:C17H19N3O3
  • Molecular Weight:313.356
  • Hs Code.:
Pyrrolidine,
1-[(hexahydro-1,3-dioxo-2-phenyl-1H-pyrrolo[1,2-c]imidazol-5-yl)carbon
yl]-

Synonyms:

Suppliers and Price of Pyrrolidine, 1-[(hexahydro-1,3-dioxo-2-phenyl-1H-pyrrolo[1,2-c]imidazol-5-yl)carbon yl]-
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Chemical Property of Pyrrolidine, 1-[(hexahydro-1,3-dioxo-2-phenyl-1H-pyrrolo[1,2-c]imidazol-5-yl)carbon yl]-
Chemical Property:
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Safty Information:
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MSDS Files:
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Technology Process of Pyrrolidine, 1-[(hexahydro-1,3-dioxo-2-phenyl-1H-pyrrolo[1,2-c]imidazol-5-yl)carbon yl]-

There total 8 articles about Pyrrolidine, 1-[(hexahydro-1,3-dioxo-2-phenyl-1H-pyrrolo[1,2-c]imidazol-5-yl)carbon yl]- 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:
Guidance literature:
Multi-step reaction with 4 steps
1: 94 percent / diethyl ether / 1 h / Heating; 1.) room temp., 15 min
2: 18percent HCl / H2O / 90 h / Heating
4: 1.) ethyl chloroformate, triethylamine / 1.) benzene, ether, 0 deg C, 15 min; 2.) benzene, ether, room temp. 20 min
With hydrogenchloride; chloroformic acid ethyl ester; triethylamine; In diethyl ether; water;
Guidance literature:
Multi-step reaction with 4 steps
1: 94 percent / diethyl ether / 1 h / Heating; 1.) room temp., 15 min
2: 18percent HCl / H2O / 90 h / Heating
4: 1.) ethyl chloroformate, triethylamine / 1.) benzene, ether, 0 deg C, 15 min; 2.) benzene, ether, room temp. 20 min
With hydrogenchloride; chloroformic acid ethyl ester; triethylamine; In diethyl ether; water;
Guidance literature:
Multi-step reaction with 3 steps
1: 18percent HCl / H2O / 90 h / Heating
3: 1.) ethyl chloroformate, triethylamine / 1.) benzene, ether, 0 deg C, 15 min; 2.) benzene, ether, room temp. 20 min
With hydrogenchloride; chloroformic acid ethyl ester; triethylamine; In water;
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