Propynyllithium
| Names | |
|---|---|
| IUPAC name
1-Lithium-1-propyne
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| Other names
1-Propyn-1-yllithium
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| Identifiers | |
3D model (JSmol)
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PubChem CID
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CompTox Dashboard (EPA)
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| Properties | |
| C3H3Li | |
| Molar mass | 46.00 g·mol−1 |
| Appearance | Whitish powder |
| Decomposition | |
| Hazards | |
| GHS labelling: | |
| GHS02: Flammable GHS05: Corrosive | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Propynyllithium is an organolithium compound with the chemical formula LiC
2CH
3. It is a white solid that is soluble in 1,2-dimethoxyethane, and tetrahydrofuran. To preclude its degradation by oxygen and water, propynyllithium and its solutions are handled under inert gas (argon or nitrogen).[1] Although commonly depicted as a monomer,
propynyllithium adopts a more complicated cluster structure as seen for many other organolithium compounds.
Synthesis
[edit | edit source]Various preparations of propynyllithium are known, but the most expeditious route starts with 1-bromopropene:[2][3]
- CH3CH=CHBr + 2 BuLi → CH3C≡CLi + 2 BuH + LiBr
Historic routes
[edit | edit source]It can be prepared by passing propyne gas through a solution of n-butyllithium[4] or by direct metallization of propyne with lithium in liquid ammonia or other solvent. Propyne, however, is an expensive gas, and, therefore, it is sometimes replaced by less expensive gas mixtures used for welding and containing a small percentage of propyne.
Applications
[edit | edit source]Propynyllithium is used in the organic synthesis as a reactant.[2][4] It is a nucleophile that adds to aldehydes to give secondary alcohols, with ketones to give tertiary alcohols, and with acid chlorides to give ketones containing the propynyl group. These reactions are used in the synthesis of complex natural and synthetic substances such as the drug mifepristone.[5]
References
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- ^ a b US 3185553, "Acetylenic lead compounds and gasoline compositions thereof"
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