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(+)-2-(4-ethylphenyl)pyrrolidine

Base Information Edit
  • Chemical Name:(+)-2-(4-ethylphenyl)pyrrolidine
  • CAS No.:1217760-03-6
  • Molecular Formula:C12H17N
  • Molecular Weight:175.274
  • Hs Code.:
  • Mol file:1217760-03-6.mol
(+)-2-(4-ethylphenyl)pyrrolidine

Synonyms:

Suppliers and Price of (+)-2-(4-ethylphenyl)pyrrolidine
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (+)-2-(4-ethylphenyl)pyrrolidine Edit
Chemical Property:
Purity/Quality:

99.00% *data from raw suppliers

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Technology Process of (+)-2-(4-ethylphenyl)pyrrolidine

There total 2 articles about (+)-2-(4-ethylphenyl)pyrrolidine 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:
tert-butyl (4-(4-ethylphenyl)-4-oxobutyl)carbamate; With trifluoroacetic acid; In dichloromethane; for 3h; Inert atmosphere; Schlenk technique;
With 1,4-diaza-bicyclo[2.2.2]octane; titanium(IV) isopropylate; bis(1,5-cyclooctadiene)diiridium(I) dichloride; (2R)-1-[(1R)-1-[bis(1,1-dimethylethyl)phosphino]ethyl]-2-[bis[4-(trifluoromethyl)phenyl]phosphino]ferrocene; hydrogen; potassium iodide; In tetrahydrofuran; toluene; at 50 ℃; for 13h; under 38002.6 Torr; Overall yield = 97 percent; Overall yield = 33.9 mg; enantioselective reaction; Autoclave;
DOI:10.1055/s-0037-1611533
Guidance literature:
tert-butyl (4-(4-ethylphenyl)-4-oxobutyl)carbamate; With trifluoroacetic acid; In dichloromethane; for 3h; Inert atmosphere; Schlenk technique;
With 1,4-diaza-bicyclo[2.2.2]octane; titanium(IV) isopropylate; bis(1,5-cyclooctadiene)diiridium(I) dichloride; (2R)-1-[(1R)-1-[bis(1,1-dimethylethyl)phosphino]ethyl]-2-[bis[4-(trifluoromethyl)phenyl]phosphino]ferrocene; hydrogen; potassium iodide; In tetrahydrofuran; toluene; at 50 ℃; for 13h; under 38002.6 Torr; Overall yield = 97 percent; Overall yield = 33.9 mg; enantioselective reaction; Autoclave;
DOI:10.1055/s-0037-1611533
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