Chemistry:Asmic
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| Names | |
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| Preferred IUPAC name
1-[(Isocyanomethyl)sulfanyl]-2-methoxybenzene | |
| Other names
Asmic; Anisyl sulfanyl methyl isocyanide
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| Identifiers | |
3D model (JSmol)
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PubChem CID
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| Properties | |
| C9H9NOS | |
| Molar mass | 179.24 g·mol−1 |
| Appearance | Off-white solid |
| Melting point | 27 °C (81 °F; 300 K) |
| Solubility in polar organic solvents | Soluble |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Anisyl sulfanyl methyl isocyanide (Asmic)[1][2] is an organic molecule that contains an isocyanide group and an ortho-methoxy-phenyl sulfide group. Asmic can be used to synthesize tri-substituted isocyanides. Asmic is a colorless to off-white solid with a melting point of 27 °C[3] that can be prepared by dehydration of the corresponding formamide by POCl3.[4][5]
Asmic can be deprotonated at the position adjacent to the isocyanide by various organic bases. The anionic form of Asmic, which is stable at low temperatures, can be alkylated with a variety of electrophiles. Two sequential deprotonation-alkylation reactions and a subsequent sulfur-lithium exchange reaction allow the synthesis of tri-substituted isocyanides.[4]
The ortho-methoxy-phenyl sulfide group is thought to facilitate deprotonation by chelating to metalated bases allowing for the base to achieve optimal trajectory during the deprotonation.[4]
Asmic can be used to prepare oxazoles by condensation reactions with esters. The ortho-methoxy-phenyl sulfide group can also undergo sulfur-lithium exchange, and likely proceeds via a 10-s-3 sulfuranide.
References
- ↑ Fleming, F. F. Composition, Synthesis, and Use of Isonitriles. U.S. Patent 8,269,032, Sept 18, 2012.
- ↑ Zhu, Jieping; Tron, Gian Cesare; Novellino, Ettore; Massarotti, Alberto; Mercalli, Valentina; Basso, Andrea; Giustiniano, Mariateresa (2017-03-06). "To each his own: isonitriles for all flavors. Functionalized isocyanides as valuable tools in organic synthesis" (in en). Chemical Society Reviews 46 (5): 1295–1357. doi:10.1039/C6CS00444J. ISSN 1460-4744. PMID 27983738. https://pubs.rsc.org/en/content/articlelanding/2017/cs/c6cs00444j.
- ↑ Abstracts of Papers, 256th ACS National Meeting & Exposition, Boston, MA, United States, August 19-23, 2018 ASMIC-driven synthesis of vinyl isocyanide
- ↑ 4.0 4.1 4.2 Alwedi, Embarek; Lujan-Montelongo, J. Armando; Pitta, Bhaskar R.; Chao, Allen; Cortés-Mejía, Rodrigo; del Campo, Jorge M.; Fleming, Fraser F. (2018-09-21). "Asmic: An Exceptional Building Block for Isocyanide Alkylations". Organic Letters 20 (18): 5910–5913. doi:10.1021/acs.orglett.8b02574. PMID 30188137.
- ↑ Shenvi, Ryan A.; Schnermann, Martin J. (2015-03-25). "Syntheses and biological studies of marine terpenoids derived from inorganic cyanide" (in en). Natural Product Reports 32 (4): 543–577. doi:10.1039/C4NP00109E. PMID 25514696.
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