(R)-2-Oxo-5-prop-2-ynyl-oxazolidine-3-carboxylic acid methyl-(2-nitro-benzyl)-amide

Base Information

Chemical Name:(R)-2-Oxo-5-prop-2-ynyl-oxazolidine-3-carboxylic acid methyl-(2-nitro-benzyl)-amide
CAS No.:474671-04-0
Molecular Formula:C₁₅H₁₅N₃O₅
Molecular Weight:317.301
Hs Code.:

Synonyms:(R)-2-Oxo-5-prop-2-ynyl-oxazolidine-3-carboxylic acid methyl-(2-nitro-benzyl)-amide

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Chemical Property of (R)-2-Oxo-5-prop-2-ynyl-oxazolidine-3-carboxylic acid methyl-(2-nitro-benzyl)-amide

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Technology Process of (R)-2-Oxo-5-prop-2-ynyl-oxazolidine-3-carboxylic acid methyl-(2-nitro-benzyl)-amide

There total 5 articles about (R)-2-Oxo-5-prop-2-ynyl-oxazolidine-3-carboxylic acid methyl-(2-nitro-benzyl)-amide 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:

: 474671-03-9
(R)-2-Oxo-5-(3-trimethylsilanyl-prop-2-ynyl)-oxazolidine-3-carboxylic acid methyl-(2-nitro-benzyl)-amide

: 474671-04-0
(R)-2-Oxo-5-prop-2-ynyl-oxazolidine-3-carboxylic acid methyl-(2-nitro-benzyl)-amide

Guidance literature:: With tetrabutyl ammonium fluoride; acetic acid; In tetrahydrofuran; at 20 ℃; for 6h;
DOI:10.1021/jo026287v

Reference yield:

: 143724-89-4
Trimethyl-((R)-3-oxiranyl-prop-1-ynyl)-silane

: 474671-04-0
(R)-2-Oxo-5-prop-2-ynyl-oxazolidine-3-carboxylic acid methyl-(2-nitro-benzyl)-amide

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium azide; ammonium chloride / aq. ethanol / 39 h / 20 °C

2.1: n-BuLi / tetrahydrofuran; hexane / 0.67 h / -78 °C

2.2: trimethylphosphine / tetrahydrofuran; hexane / 4.33 h / -78 - 20 °C

3.1: lithium hexamethyldisilazide / tetrahydrofuran / 6 h / -78 - 20 °C

4.1: Bu₄NF; acetic acid / tetrahydrofuran / 6 h / 20 °C

With n-butyllithium; sodium azide; ammonium chloride; tetrabutyl ammonium fluoride; acetic acid; lithium hexamethyldisilazane; In tetrahydrofuran; ethanol; hexane;
DOI:10.1021/jo026287v

Reference yield:

: 455312-10-4
(R)-5-(3-Trimethylsilanyl-prop-2-ynyl)-oxazolidin-2-one

: 474671-04-0
(R)-2-Oxo-5-prop-2-ynyl-oxazolidine-3-carboxylic acid methyl-(2-nitro-benzyl)-amide

Guidance literature:: Multi-step reaction with 2 steps

1: lithium hexamethyldisilazide / tetrahydrofuran / 6 h / -78 - 20 °C

2: Bu₄NF; acetic acid / tetrahydrofuran / 6 h / 20 °C

With tetrabutyl ammonium fluoride; acetic acid; lithium hexamethyldisilazane; In tetrahydrofuran;
DOI:10.1021/jo026287v