(2R,4R)-3-Benzoyl-4-benzyl-4-(2-methanesulfinyl-ethyl)-2-phenyl-oxazolidin-5-one

Base Information

Chemical Name:(2R,4R)-3-Benzoyl-4-benzyl-4-(2-methanesulfinyl-ethyl)-2-phenyl-oxazolidin-5-one
CAS No.:769953-14-2
Molecular Formula:C₂₆H₂₅NO₄S
Molecular Weight:447.555
Hs Code.:

Synonyms:(2R,4R)-3-Benzoyl-4-benzyl-4-(2-methanesulfinyl-ethyl)-2-phenyl-oxazolidin-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 (2R,4R)-3-Benzoyl-4-benzyl-4-(2-methanesulfinyl-ethyl)-2-phenyl-oxazolidin-5-one

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Technology Process of (2R,4R)-3-Benzoyl-4-benzyl-4-(2-methanesulfinyl-ethyl)-2-phenyl-oxazolidin-5-one

There total 1 articles about (2R,4R)-3-Benzoyl-4-benzyl-4-(2-methanesulfinyl-ethyl)-2-phenyl-oxazolidin-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: 94.0%

: 769953-07-3
(2R,4R)-3-benzoyl-4-benzyl-4-(2-methylsulfanyl-ethyl)-2-phenyl-oxazolidin-5-one

: 769953-14-2
(2R,4R)-3-Benzoyl-4-benzyl-4-(2-methanesulfinyl-ethyl)-2-phenyl-oxazolidin-5-one

Guidance literature:: With dihydrogen peroxide; In acetic acid; at 20 ℃; for 4h;
DOI:10.1039/b406450j

Reference yield: 93.0%

: 769953-14-2
(2R,4R)-3-Benzoyl-4-benzyl-4-(2-methanesulfinyl-ethyl)-2-phenyl-oxazolidin-5-one

: 769953-08-4
(2R,4R)-3-benzoyl-4-benzyl-2-phenyl-4-vinyl-oxazolidin-5-one

Guidance literature:: In m-xylene; at 200 ℃; for 16h;
DOI:10.1039/b406450j

Reference yield:

: 769953-14-2
(2R,4R)-3-Benzoyl-4-benzyl-4-(2-methanesulfinyl-ethyl)-2-phenyl-oxazolidin-5-one

: 769953-11-9
(2R)-1-benzoyl-2-benzyl-2,5-dihydro-1H-pyrrole-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 93 percent / m-xylene / 16 h / 200 °C

2: 99 percent / aq. NaOH / methanol / 1 h / Heating

3: 100 percent / diethyl ether / 2 h / 20 °C

4: 31 percent / NaH / dimethylformamide / 2 h / 0 - 20 °C

5: 94 percent / (CH₃)2C=CHCH=Ru(PCy₃)2Cl₂ / benzene / 16 h / Heating

With sodium hydroxide; sodium hydride; ruthenium(II) dichloro(3-methyl-1,2-butenylidene)bis(tricyclohexylphosphine); In methanol; diethyl ether; N,N-dimethyl-formamide; m-xylene; benzene;
DOI:10.1039/b406450j