methyl (2S,3R,4S,5R)-4-benzoyl-3-phenyl-5-(4-chlorophenyl)pyrrolidine-2-carboxylate

Base Information

Chemical Name:methyl (2S,3R,4S,5R)-4-benzoyl-3-phenyl-5-(4-chlorophenyl)pyrrolidine-2-carboxylate
CAS No.:1221295-27-7
Molecular Formula:C₂₅H₂₂ClNO₃
Molecular Weight:419.908
Hs Code.:

Synonyms:methyl (2S,3R,4S,5R)-4-benzoyl-3-phenyl-5-(4-chlorophenyl)pyrrolidine-2-carboxylate

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Chemical Property of methyl (2S,3R,4S,5R)-4-benzoyl-3-phenyl-5-(4-chlorophenyl)pyrrolidine-2-carboxylate

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Technology Process of methyl (2S,3R,4S,5R)-4-benzoyl-3-phenyl-5-(4-chlorophenyl)pyrrolidine-2-carboxylate

There total 2 articles about methyl (2S,3R,4S,5R)-4-benzoyl-3-phenyl-5-(4-chlorophenyl)pyrrolidine-2-carboxylate 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: 81.0%

: 76862-09-4
methyl N-(4-chlorobenzylidene)glycinate

: 94-41-7
benzalacetophenone

: 1221295-27-7
methyl (2S,3R,4S,5R)-4-benzoyl-3-phenyl-5-(4-chlorophenyl)pyrrolidine-2-carboxylate

: methyl 4-benzoyl-3-phenyl-5-(4-chlorophenyl)pyrrolidine-2-carboxylate

Guidance literature:: With C₃₄H₃₃FeN₂PS; silver(I) acetate; triethylamine; In 1,2-dichloro-ethane; at -10 ℃; for 2h; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1021/ol1024647

Reference yield:

: 76862-09-4
(E)-methyl 2-((4-chlorobenzylidene)amino)acetate

: 614-47-1
1,3-diphenyl-propen-3-one

: 1221295-27-7
methyl (2S,3R,4S,5R)-4-benzoyl-3-phenyl-5-(4-chlorophenyl)pyrrolidine-2-carboxylate

: methyl 4-benzoyl-5-(4-chlorophenyl)-3-phenylpyrrolidine-2-carboxylate

Guidance literature:: With brucine diol; silver fluoride; 1,8-diazabicyclo[5.4.0]undec-7-ene; tert-butyl alcohol; In tetrahydrofuran; at -15 ℃; Overall yield = 50 %; Overall yield = 105 mg; enantioselective reaction; Inert atmosphere;
DOI:10.1002/adsc.201500958