From Surf Wiki (app.surf) — the open knowledge base
N-Methylformamide
NMF
N-Methylformamide (NMF) is a colorless, nearly odorless, organic compound and secondary amide with molecular formula , which is a liquid at room temperature. NMF is mainly used as a reagent in various organic syntheses with limited applications as a highly polar solvent.
NMF is closely related to other formamides, notably formamide and dimethylformamide (DMF). However, industrial use and production of NMF are far less than for either of these other formamides. DMF is favored over NMF as a solvent due to its greater stability. Annual production of NMF can be assumed to be significantly less than the production of either formamide (100,000 tons) or DMF (500,000 tons).
Structure and properties
Because of slow rotation about the N-C(O) bond, NMF exists as two rotamers that can be distinguished by NMR spectroscopy. The two principal resonance structures for one of these rotamers is shown: ::[[Image:NMFresonanceStr's.png|220px|Principal resonance structures for one rotamer of NMF]]
This description highlights the partial double bond that exists between the carbonyl carbon and nitrogen, which raises the rotational barrier. Thus, the molecule is not able to freely rotate around its main axis and the (E)-configuration is preferred due to steric repulsion of the larger substituents.
This molecule has been tentatively identified in interstellar space by the ALMA radio telescope. It may have formed on dust grains. This could prove to be a key molecule for interstellar pre-biotic chemistry due to its peptide bond.
Preparation
NMF is typically prepared by allowing methylamine to react with methyl formate: :
A less common alternative to this process is transamidation involving formamide: :
Uses
NMF is a specialized solvent in oil refineries. It is a precursor in specialized amidation reactions where formamide would not be suitable. These reactions can generally be categorized by the following equation: : (Where Lg is a leaving group).
Laboratory uses
NMF is the precursor to methyl isocyanide, a ligand in coordination chemistry. NMF is used as a solvent in aluminum electrolytic capacitors.
References
References
- Bipp, H.. "Formamides".
- (October 1995). "Hydration of cis and trans N‐methylformamide as revealed by the use of 17 O‐NMR, molecular mechanics, and ab initio calculations". Biopolymers.
- Schuster, R. E.. (1966). "Methyl Isocyanide".
This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page.
Ask Mako anything about N-Methylformamide — get instant answers, deeper analysis, and related topics.
Research with MakoFree with your Surf account
Create a free account to save articles, ask Mako questions, and organize your research.
Sign up freeThis content may have been generated or modified by AI. CloudSurf Software LLC is not responsible for the accuracy, completeness, or reliability of AI-generated content. Always verify important information from primary sources.
Report