(4S,5R)-3-[(2S,3S)-2-Benzyloxymethyl-1-(bis-trimethylsilanyl-methyl)-4-oxo-azetidin-3-yl]-4,5-diphenyl-oxazolidin-2-one

Base Information

Chemical Name:(4S,5R)-3-[(2S,3S)-2-Benzyloxymethyl-1-(bis-trimethylsilanyl-methyl)-4-oxo-azetidin-3-yl]-4,5-diphenyl-oxazolidin-2-one
CAS No.:198022-19-4
Molecular Formula:C₃₃H₄₂N₂O₄Si₂
Molecular Weight:586.878
Hs Code.:

Synonyms:(4S,5R)-3-[(2S,3S)-2-Benzyloxymethyl-1-(bis-trimethylsilanyl-methyl)-4-oxo-azetidin-3-yl]-4,5-diphenyl-oxazolidin-2-one

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Chemical Property of (4S,5R)-3-[(2S,3S)-2-Benzyloxymethyl-1-(bis-trimethylsilanyl-methyl)-4-oxo-azetidin-3-yl]-4,5-diphenyl-oxazolidin-2-one

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Technology Process of (4S,5R)-3-[(2S,3S)-2-Benzyloxymethyl-1-(bis-trimethylsilanyl-methyl)-4-oxo-azetidin-3-yl]-4,5-diphenyl-oxazolidin-2-one

There total 6 articles about (4S,5R)-3-[(2S,3S)-2-Benzyloxymethyl-1-(bis-trimethylsilanyl-methyl)-4-oxo-azetidin-3-yl]-4,5-diphenyl-oxazolidin-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: 70.0%

: 180072-69-9
[2-Benzyloxy-eth-(E)-ylidene]-(bis-trimethylsilanyl-methyl)-amine

: 198021-41-9
[(4S,5R)-2-oxo-4,5-diphenyloxazolidin-3-yl]acetyl chloride

: 198022-19-4
(4S,5R)-3-[(2S,3S)-2-Benzyloxymethyl-1-(bis-trimethylsilanyl-methyl)-4-oxo-azetidin-3-yl]-4,5-diphenyl-oxazolidin-2-one

Guidance literature:: With triethylamine; In chloroform; for 20h; Heating;
DOI:10.1002/chem.19970030909

Reference yield:

: 23204-70-8
(4S,5R)-4,5-diphenyl-1,3-oxazolidin-2-one

: 198022-19-4
(4S,5R)-3-[(2S,3S)-2-Benzyloxymethyl-1-(bis-trimethylsilanyl-methyl)-4-oxo-azetidin-3-yl]-4,5-diphenyl-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 4 steps

1: NaH / tetrahydrofuran / 2 h / 0 °C

2: aq. NaOH / tetrahydrofuran / 2 h / Ambient temperature

3: 98 percent / (COCl)2, DMF / CH₂Cl₂ / 1 h / Ambient temperature

4: 70 percent / NEt₃, MS 4A / CHCl₃ / 20 h / Heating

With sodium hydroxide; oxalyl dichloride; sodium hydride; triethylamine; N,N-dimethyl-formamide; In tetrahydrofuran; dichloromethane; chloroform;
DOI:10.1002/chem.19970030909

Reference yield:

: 60656-87-3
benzyloxyacetoaldehyde

: 198022-19-4
(4S,5R)-3-[(2S,3S)-2-Benzyloxymethyl-1-(bis-trimethylsilanyl-methyl)-4-oxo-azetidin-3-yl]-4,5-diphenyl-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / MS 4A / CH₂Cl₂ / 0.5 h / 20 °C

2: 70 percent / NEt₃, MS 4A / CHCl₃ / 20 h / Heating

With triethylamine; In dichloromethane; chloroform;
DOI:10.1002/chem.19970030909