(3R,4R)-1-Benzyl-3-((R)-2,2-dimethyl-4-phenyl-oxazolidin-3-yl)-4-methyl-azetidin-2-one

Base Information

Chemical Name:(3R,4R)-1-Benzyl-3-((R)-2,2-dimethyl-4-phenyl-oxazolidin-3-yl)-4-methyl-azetidin-2-one
CAS No.:124716-37-6
Molecular Formula:C₂₂H₂₆N₂O₂
Molecular Weight:350.461
Hs Code.:

Synonyms:(3R,4R)-1-Benzyl-3-((R)-2,2-dimethyl-4-phenyl-oxazolidin-3-yl)-4-methyl-azetidin-2-one

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Chemical Property of (3R,4R)-1-Benzyl-3-((R)-2,2-dimethyl-4-phenyl-oxazolidin-3-yl)-4-methyl-azetidin-2-one

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Technology Process of (3R,4R)-1-Benzyl-3-((R)-2,2-dimethyl-4-phenyl-oxazolidin-3-yl)-4-methyl-azetidin-2-one

There total 2 articles about (3R,4R)-1-Benzyl-3-((R)-2,2-dimethyl-4-phenyl-oxazolidin-3-yl)-4-methyl-azetidin-2-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:

: 201230-82-2
carbon monoxide

: 34233-75-5
N-ethylidenebenzylamine

: 124716-37-6,124816-63-3,134679-63-3,134679-72-4
(S)-1-Benzyl-3-((S)-2,2-dimethyl-4-phenyl-oxazolidin-3-yl)-4-methyl-azetidin-2-one

Guidance literature:: In dichloromethane; for 17h; under 760 Torr; Yield given; Irradiation;
DOI:10.1021/ja00015a036

Reference yield:

: 201230-82-2
carbon monoxide

: 34233-75-5
N-ethylidenebenzylamine

: 112044-00-5
N-formyl acetonide of (R)-phenylglycinol

: 124816-63-3
(3R,4S)-1-Benzyl-3-((R)-2,2-dimethyl-4-phenyl-oxazolidin-3-yl)-4-methyl-azetidin-2-one

: 124716-37-6
(3R,4R)-1-Benzyl-3-((R)-2,2-dimethyl-4-phenyl-oxazolidin-3-yl)-4-methyl-azetidin-2-one

Guidance literature:: With chloro-trimethyl-silane; disodium pentacarbonylchromium; Yield given. Multistep reaction. Yields of byproduct given; 2.) Et₂O, 60 psi, 24 h, irrad.;
DOI:10.1021/ja00159a034