N-Methylmorpholine N-oxide

Technopedia Center

Faculty of Engineering and Computer Science
S1 Informatics S1 Information Systems S1 Information Technology S1 Computer Engineering S1 Electrical Engineering S1 Civil Engineering

faculty of Economics and Business
S1 Management S1 Accountancy

Faculty of Letters and Educational Sciences
S1 English literature S1 English language education S1 Mathematics education S1 Sports Education

N-Methylmorpholine N-oxide - Wikipedia

From Wikipedia, the free encyclopedia

(Redirected from N-methylmorpholine N-oxide)

N-Methylmorpholine N-oxide

Identifiers

CAS Number

7529-22-8^Y

3D model (JSmol)

Interactive image

ChEBI

CHEBI:52093^Y

ChemSpider

74032^Y

ECHA InfoCard

100.028.538

PubChem CID

82029

UNII

ARC64PKJ0F^Y

CompTox Dashboard (EPA)

DTXSID3029287

InChI

InChI=1S/C5H11NO2/c1-6(7)2-4-8-5-3-6/h2-5H2,1H3^Y
Key: LFTLOKWAGJYHHR-UHFFFAOYSA-N^Y
InChI=1/C5H11NO2/c1-6(7)2-4-8-5-3-6/h2-5H2,1H3
Key: LFTLOKWAGJYHHR-UHFFFAOYAV

SMILES

C[N+]1(CCOCC1)[O-]

Properties

Chemical formula

C₅H₁₁NO₂

Molar mass

117.15 g/mol

Melting point

180 to 184 °C (356 to 363 °F; 453 to 457 K)

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

verify (what is ^YN ?)

Infobox references

N-Methylmorpholine N-oxide (more correctly 4-methylmorpholine 4-oxide), NMO or NMMO is an organic compound. This heterocyclic amine oxide and morpholine derivative is used in organic chemistry as a co-oxidant and sacrificial catalyst in oxidation reactions for instance in osmium tetroxide oxidations and the Sharpless asymmetric dihydroxylation or oxidations with TPAP.^[1] NMO is commercially supplied both as a monohydrate C₅H₁₁NO₂·H₂O and as the anhydrous compound. The monohydrate is used as a solvent for cellulose in the lyocell process to produce cellulose fibers.

Uses

Solvent of cellulose

NMMO monohydrate is used as a solvent in the lyocell process to produce lyocell fiber.^[2]^[3] It dissolves cellulose to form a solution called dope, and the cellulose is reprecipitated in a water bath to produce a fiber. The process is similar but not analogous to the viscose process. In the viscose process, cellulose is made soluble by conversion to its xanthate derivatives. With NMMO, cellulose is not derivatized but dissolves to give a homogeneous polymer solution. The resulting fiber is similar to viscose; this was observed, for example, for Valonia cellulose microfibrils. Dilution with water causes the cellulose to reprecipitate, i.e. the solvation of cellulose with NMMO is a water sensitive process.^[4]

Cellulose remains insoluble in most solvents because it has a strong and highly structured intermolecular hydrogen bonding network, which resists common solvents. NMMO breaks the hydrogen bonding network that keeps cellulose insoluble in water and other solvents. Similar solubility has been obtained in a few solvents, particularly a mix of lithium chloride in dimethyl acetamide and some hydrophilic ionic liquids.

Dissolution of scleroproteins

Another use of NMMO is in the dissolution of scleroprotein (found in animal tissue). This dissolution occurs in the crystal areas which are more homogeneous and contain glycine and alanine residues with a small number of other residues. How NMMO dissolves these proteins is scarcely studied. Other studies, however, have been done in similar amide systems (i.e. hexapeptide). The hydrogen bonds of the amides can be broken by NMMO.^[5]

Oxidant

NMO, as an N-oxide, is an oxidant in the Upjohn dihydroxylation. It is generally used in stoichiometric amounts as a secondary oxidant (a cooxidant) to regenerate a primary (catalytic) oxidant after the latter has been reduced by the substrate. Vicinal syn-dihydroxylation reactions for example, would, in theory, require stoichiometric amounts of toxic, volatile and expensive osmium tetroxide, but if continuously regenerated with NMO, the amount required can be reduced to catalytic quantities.

References

^ Mark R. Sivik and Scott D. Edmondson "N-Methylmorpholine N-Oxide" E-EROS ENCYCLOPEDIA OF REAGENTS FOR ORGANIC SYNTHESIS, 2008 doi:10.1002/047084289X.rm216.pub2
^ Rosenau, Thomas; Potthast, Antje; Sixta, Herbert; Kosma, Paul (2001). "The chemistry of side reactions and byproduct formation in the system NMMO/cellulose (Lyocell process)". Progress in Polymer Science. 26 (9). doi:10.1016/S0079-6700(01)00023-5. Retrieved 8 December 2024.
^ Hans Krässig, Josef Schurz, Robert G. Steadman, Karl Schliefer, Wilhelm Albrecht, Marc Mohring, Harald Schlosser "Cellulose" in Ullmann's Encyclopedia of Industrial Chemistry, 2002, Wiley-VCH, Weinheim. doi:10.1002/14356007.a05_375.pub2
^ Noé, Pierre, and Henri Chanzy "Swelling of Valonia cellulose microfibrils in amine oxide systems." Canadian Journal of Chemistry Volume 86 issue 6 pages 520-524(2008). retrieved via EBSCO, Advanced Placement Source. 11 Nov. 2009.
^ E. S. Sashina, N. P. Novoselov, S. V.Toroshekova, V. E. Petrenko, "Quantum-chemical study of the mechanism of dissolution of scleroproteins in N-methylmorpholine N-oxide." Russian Journal of General Chemistry volume78 issue 1 pages 139-145 (2008). retrieved via EBSCO, Advanced Placement Source. 11 Nov. 2009.
^ Preparation of 3H-Pyrrolo[2,3-c]isoquinolines and 3H-Pyrrolo[2,3-c][2,6]- and 3H-Pyrrolo[2,3-c][1,7]-naphthyridines U. Narasimha Rao, Xuemei Han and Edward R. Biehl Arkivoc 2002 (x) 61-66 online article

Categories:

Hidden categories: