(1S,3R,4S)-endo-3-(3-chlorophenyl)-2-phenyl-2-azabicyclo[2.2.2]octan-5-one

Base Information

Chemical Name:(1S,3R,4S)-endo-3-(3-chlorophenyl)-2-phenyl-2-azabicyclo[2.2.2]octan-5-one
CAS No.:1427441-69-7
Molecular Formula:C₁₉H₁₈ClNO
Molecular Weight:311.811
Hs Code.:

Synonyms:(1S,3R,4S)-endo-3-(3-chlorophenyl)-2-phenyl-2-azabicyclo[2.2.2]octan-5-one

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

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Chemical Property of (1S,3R,4S)-endo-3-(3-chlorophenyl)-2-phenyl-2-azabicyclo[2.2.2]octan-5-one

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Technology Process of (1S,3R,4S)-endo-3-(3-chlorophenyl)-2-phenyl-2-azabicyclo[2.2.2]octan-5-one

There total 2 articles about (1S,3R,4S)-endo-3-(3-chlorophenyl)-2-phenyl-2-azabicyclo[2.2.2]octan-5-one 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:

: 930-68-7
cyclohexenone

: 32347-04-9,5877-57-6
N-(3-chlorobenzylidene)aniline

: 1427441-69-7
(1S,3R,4S)-endo-3-(3-chlorophenyl)-2-phenyl-2-azabicyclo[2.2.2]octan-5-one

: exo-3-(3-chlorophenyl)-2-phenyl-2-azabicyclo[2.2.2]octan-5-one

: (1R,3S,4R)-endo-3-(3-chlorophenyl)-2-phenyl-2-azabicyclo[2.2.2]octan-5-one

Guidance literature:: With C₂₆H₃₀CoN₂O₆^(1-)*H⁽¹⁺⁾; In tetrachloromethane; at 20 ℃; for 48h; Overall yield = 52 %Spectr.; stereoselective reaction; Inert atmosphere; Schlenk technique;
DOI:10.1016/j.tetasy.2013.01.011

Reference yield:

: 930-68-7
cyclohexenone

: 32347-04-9,5877-57-6
N-(3-chlorobenzylidene)aniline

: 1427441-69-7
(1S,3R,4S)-endo-3-(3-chlorophenyl)-2-phenyl-2-azabicyclo[2.2.2]octan-5-one

: C₁₉H₁₈ClNO

Guidance literature:: cyclohexenone; With Merrifield resin loaded proline modified dendrigraft second generation polyepichlorohydrin polymer supported copper complex; In tetrachloromethane; for 0.0333333h;

N-(3-chlorobenzylidene)aniline; In tetrachloromethane; at 30 ℃; for 3h; Overall yield = 89 %; stereoselective reaction;
DOI:10.1039/c6ra15548k