{[(4S)-4-methyl-2-oxo-1,3-oxazolidin-4-yl]methyl}(triphenyl)phosphonium iodide

Base Information

Chemical Name:{[(4S)-4-methyl-2-oxo-1,3-oxazolidin-4-yl]methyl}(triphenyl)phosphonium iodide
CAS No.:1618092-42-4
Molecular Formula:C₂₃H₂₃NO₂P*I
Molecular Weight:503.319
Hs Code.:

Synonyms:{[(4S)-4-methyl-2-oxo-1,3-oxazolidin-4-yl]methyl}(triphenyl)phosphonium iodide

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Chemical Property of {[(4S)-4-methyl-2-oxo-1,3-oxazolidin-4-yl]methyl}(triphenyl)phosphonium iodide

Chemical Property:

Purity/Quality:

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Technology Process of {[(4S)-4-methyl-2-oxo-1,3-oxazolidin-4-yl]methyl}(triphenyl)phosphonium iodide

There total 8 articles about {[(4S)-4-methyl-2-oxo-1,3-oxazolidin-4-yl]methyl}(triphenyl)phosphonium iodide 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: 57.0%

: 1618092-41-3
(4S)-4-(iodomethyl)-4-methyl-1,3-oxazolidin-2-one

: 603-35-0
triphenylphosphine

: 1618092-42-4
{[(4S)-4-methyl-2-oxo-1,3-oxazolidin-4-yl]methyl}(triphenyl)phosphonium iodide

Guidance literature:: In N,N-dimethyl-formamide; at 110 ℃; for 3h;
DOI:10.1016/j.tet.2014.05.086

Reference yield:

: 1312772-35-2
methyl [(2S)-1-(benzyloxy)-3-hydroxy-2-methylpropan-2-yl]carbamate

: 1618092-42-4
{[(4S)-4-methyl-2-oxo-1,3-oxazolidin-4-yl]methyl}(triphenyl)phosphonium iodide

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium tert-butylate / tetrahydrofuran / 3 h / 20 °C

2.1: potassium carbonate; palladium 10% on activated carbon; hydrogen / ethanol / 3 h

3.1: pyridine; p-toluenesulfonyl chloride / 3 h / 20 °C

3.2: 12 h / Reflux

4.1: N,N-dimethyl-formamide / 3 h / 110 °C

With pyridine; palladium 10% on activated carbon; potassium tert-butylate; hydrogen; potassium carbonate; p-toluenesulfonyl chloride; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.tet.2014.05.086

Reference yield:

: methyl (2R,4R)-4-[(benzyloxy)methyl]-2-tert-butyl-4-methyl-1,3-oxazolidine-3-carboxylate

: 1618092-42-4
{[(4S)-4-methyl-2-oxo-1,3-oxazolidin-4-yl]methyl}(triphenyl)phosphonium iodide

Guidance literature:: Multi-step reaction with 5 steps

1.1: toluene-4-sulfonic acid / methanol / 1 h / Reflux

2.1: potassium tert-butylate / tetrahydrofuran / 3 h / 20 °C

3.1: potassium carbonate; palladium 10% on activated carbon; hydrogen / ethanol / 3 h

4.1: pyridine; p-toluenesulfonyl chloride / 3 h / 20 °C

4.2: 12 h / Reflux

5.1: N,N-dimethyl-formamide / 3 h / 110 °C

With pyridine; palladium 10% on activated carbon; potassium tert-butylate; hydrogen; potassium carbonate; toluene-4-sulfonic acid; p-toluenesulfonyl chloride; In tetrahydrofuran; methanol; ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.tet.2014.05.086