(2S,3R,4S,5R)-methyl 4-acetyl-5-(4-chlorophenyl)-3-phenylpyrrolidine-2-carboxylate

Base Information

Chemical Name:(2S,3R,4S,5R)-methyl 4-acetyl-5-(4-chlorophenyl)-3-phenylpyrrolidine-2-carboxylate
CAS No.:1221295-26-6
Molecular Formula:C₂₀H₂₀ClNO₃
Molecular Weight:357.837
Hs Code.:

Synonyms:(2S,3R,4S,5R)-methyl 4-acetyl-5-(4-chlorophenyl)-3-phenylpyrrolidine-2-carboxylate

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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 (2S,3R,4S,5R)-methyl 4-acetyl-5-(4-chlorophenyl)-3-phenylpyrrolidine-2-carboxylate

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Technology Process of (2S,3R,4S,5R)-methyl 4-acetyl-5-(4-chlorophenyl)-3-phenylpyrrolidine-2-carboxylate

There total 2 articles about (2S,3R,4S,5R)-methyl 4-acetyl-5-(4-chlorophenyl)-3-phenylpyrrolidine-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: 85.0%

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

: 1896-62-4
(E)-benzalacetone

: 1221295-26-6
(2S,3R,4S,5R)-methyl 4-acetyl-5-(4-chlorophenyl)-3-phenylpyrrolidine-2-carboxylate

Guidance literature:: With C₃₆H₃₆FeN₃PS; silver(I) acetate; triethylamine; In dichloromethane; at 0 ℃; for 5h; optical yield given as %ee; enantioselective reaction;
DOI:10.1021/ol100336q

Reference yield:

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

: 1896-62-4
(E)-benzalacetone

: 1221295-26-6
(2S,3R,4S,5R)-methyl 4-acetyl-5-(4-chlorophenyl)-3-phenylpyrrolidine-2-carboxylate

: 1221295-50-6
(2S,3R,4S,5R)-methyl 4-acetyl-5-(4-chlorophenyl)-3-phenylpyrrolidine-2-carboxylate

Guidance literature:: With C₃₄H₃₂FeN₃PS; silver trifluoromethanesulfonate; triethylamine; In toluene; at 20 ℃; for 12h; optical yield given as %ee; enantioselective reaction;
DOI:10.1021/ol100336q