methyl (2'S,3R)-(-)-5-<2-(methoxymethyl)pyrrolidinoimino>-3-phenylpentanoate

Base Information

Chemical Name:methyl (2'S,3R)-(-)-5-<2-(methoxymethyl)pyrrolidinoimino>-3-phenylpentanoate
CAS No.:107985-91-1
Molecular Formula:C₁₈H₂₆N₂O₃
Molecular Weight:318.416
Hs Code.:

Synonyms:methyl (2'S,3R)-(-)-5-<2-(methoxymethyl)pyrrolidinoimino>-3-phenylpentanoate

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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 methyl (2'S,3R)-(-)-5-<2-(methoxymethyl)pyrrolidinoimino>-3-phenylpentanoate

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Technology Process of methyl (2'S,3R)-(-)-5-<2-(methoxymethyl)pyrrolidinoimino>-3-phenylpentanoate

There total 2 articles about methyl (2'S,3R)-(-)-5-<2-(methoxymethyl)pyrrolidinoimino>-3-phenylpentanoate 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:

: 59983-39-0,187035-29-6
(S)-1-amino-2-(methoxymethyl)pyrrolidine

: 107985-91-1
methyl (2'S,3R)-(-)-5-<2-(methoxymethyl)pyrrolidinoimino>-3-phenylpentanoate

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / Ambient temperature

2: 1.) nBuLi, diisopropylamine / 1.) THF, hexane, 0 deg C, 2 h; 2.) -78 deg C, 2 h; -78 deg C up to 0 deg C, 12 h

With n-butyllithium; diisopropylamine;

Reference yield:

: 103-26-4,1754-62-7
Methyl cinnamate

: 107985-85-3
(S)-(-)-1-(ethylideneamino)-2-(methoxymethyl)pyrrolidine

: 107985-91-1
methyl (2'S,3R)-(-)-5-<2-(methoxymethyl)pyrrolidinoimino>-3-phenylpentanoate

: (S)-5-[(E)-(S)-2-Methoxymethyl-pyrrolidin-1-ylimino]-3-phenyl-pentanoic acid methyl ester

Guidance literature:: With n-butyllithium; diisopropylamine; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts; 1.) THF, hexane, 0 deg C, 2 h; 2.) -78 deg C, 2 h; -78 deg C up to 0 deg C, 12 h;