(S)-4-Methyl-2,5-oxazolidonedione Chemical Properties

Melting point:

92℃

alpha 

+5.13°(25/D,c=6.4,dioxane)

Density 

1.296

storage temp. 

Inert atmosphere,Store in freezer, under -20°C

solubility 

DMSO (Very Slightly, Heated)

form 

Solid

pka

9.38±0.40(Predicted)

color 

White to Off-White

InChI

InChI=1S/C4H5NO3/c1-2-3(6)8-4(7)5-2/h2H,1H3,(H,5,7)/t2-/m0/s1

InChIKey

DTETYCNJKAUROO-REOHCLBHSA-N

SMILES

O1C(=O)[C@H](C)NC1=O

Safety Information

HS Code 

2934999090

(S)-4-Methyl-2,5-oxazolidonedione Usage And Synthesis

Description

(S)-4-Methyl-2,5-oxazolidonedione is also known as N-Carboxy anhydrides. The Fuchs-Farthing method, reported in 1922, was the only practical method for preparing (S)-4-Methyl-2,5-oxazolidonedione[1]. N-Carboxy anhydrides (NCAs) are important as α-amino acid building blocks for the synthesis of oligopeptides and nonpeptide compounds, and for the synthesis of polypeptides[2]. The polymerization of NCAs is the main process for the preparation of polypeptides, and its purity and side chains can significantly affect the synthesized polypeptides. NCAs polymerizations have been initiated using many different nucleophiles and bases, the most common being primary amines and alkoxide anions[3].

Uses

(S)-4-Methyl-2,5-oxazolidonedione is composed of oxazolidine ring and 2,5-dione ring. It exhibits chirality, meaning it exists as two non-superimposable mirror image forms. Therefore, it can be used as an organic reagent for the synthesis of enantiomeric pure substances. (S)-4-Methyl-2,5-oxazolidonedione is a reagent used in the synthesis of poly(γ-benzyl-L-glutamate) and its block polypeptides with alanine, leucine and phenylalanine.

Production Methods

L-alanine (20.0 g, 0.224 mol) and triphosgene (53.4 g, 0.180 mol) were suspended in 400.0 mL of dry THF bubbled with nitrogen flux in a flame-dried three-neck flask. The mixture was stirred at 60 °C for 2 h before further bubbling with nitrogen flux for 30 min. After that, the solution was precipitated in 1000.0 mL of n-hexane and stored at -20 °C. The supernatant was removed, and the residues were collected and dissolved in 200.0 mL of ethyl acetate, before two washings with 100.0mL of ice-cold water and one washing with 100.0 mL of 0.5% NaHCO3 ice-cold aqueous solution. The organic phase was then dried over anhydrous MgSO4 and evaporated to obtain 15.5 g of L-Ala NCA ((S)-4-Methyl-2,5-oxazolidonedione). The yield of L-Ala NCA was 77.5%.

Synthesis Reference(s)

The Journal of Organic Chemistry, 50, p. 2200, 1985 DOI: 10.1021/jo00212a042

References

[1] Otake Y, et al. Rapid and Mild Synthesis of Amino Acid N-Carboxy Anhydrides Using Basic-to-Acidic Flash Switching in a Micro-flow Reactor. Angewandte Chemie International Edition, 2018; 57: 11389-11393.
[2] Sch?fer G, et al. Synthesis of Sterically Hindered N-Acylated Amino Acids from N-Carboxyanhydrides. Organic Letters, 2014; 16: 1526–1529.
[3] Imanishi Y, et al. Polymerization of α-amino acid N-carboxyanhydride in the presence of preformed poly(α-amino acid) - from chain effect to stereoselective polymerization. Pure and Applied Chemistry, 1981; 53.

(S)-4-Methyl-2,5-oxazolidonedione(2224-52-4)Related Product Information

• FMOC-ALA-N-CARBOXYANHYDRIDE
• Ethyl (S)-2-[(S)-4-methyl-2,5-dioxo-1,3-oxazolidin-3-yl]-4-phenylbutyrate
• 3-(3,5-DICHLOROPHENYL)-5-ETHENYL-5-METHYL-2,4-OXAZOLIDINEDIONE,(+or-)-3-(3,5-dichlorophenyl)-5-ethenyl-5-methyl-2,4-oxazolidinedion
• 5-METHYL-2,4-OXAZOLIDINEDIONE
• FMOC-GLU(OTBU)-N-CARBOXYANHYDRIDE
• BOC-O-BENZYL-L-SERINE N-CARBOXY ANHYDRIDE
• NALPHA-9-Fluorenylmethoxycarbonyl-L-leucine N-carboxylic anhydride
• BOC-ASP(OBZL)-N-CARBOXYANHYDRIDE
• BOC-L-ALANINE-NCA
• N-α-Fmoc-N-γ-trityl-L-asparagine N-carboxyanhydride
• BOC-O-BENZYL-L-THREONINE N-CARBOXY ANHYDRIDE
• FMOC-L-VALINE N-CARBOXY ANHYDRIDE
• N-α-Boc-N-ε-Z-L-lysine N-carboxyanhydride
• Fmoc-O-tert·butyl-L-threonineN-carboxyanhydride
• FMOC-ILE-N-CARBOXYANHYDRIDE
• BOC-TRYPTOPHAN NCA
• N-tert-Butoxycarbonyl-L-leucine N-carboxylic anhydride
• BOC-ILE-N-CARBOXYANHYDRIDE