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| CAS No.: | 917-54-4 |
|---|---|
| Name: | METHYLLITHIUM |
| Article Data: | 43 |
| Molecular Structure: | |
|
|
|
| Formula: | CH3Li |
| Molecular Weight: | 21.9758 |
| Synonyms: | Lithiummethide; |
| EINECS: | 213-026-4 |
| Density: | 0.85 g/mL at 20 °C |
| Melting Point: | 70-71oC |
| Boiling Point: | 35oC |
| Flash Point: | 5°F |
| Solubility: | Reacts with water. |
| Appearance: | colorless to yellowish solution |
| Hazard Symbols: |
 F+, C, N, F
|
| Risk Codes: | 12-15-17-22-34-66-67-65-51/53-11 |
| Safety: | 16-26-36/37/39-45-43-30-60 |
| Transport Information: | UN 3399 4.3/PG 1 |
| PSA: | 0.00000 |
| LogP: | 0.58380 |
- 958254-66-51H-Imidazo[4,5-b]pyridine-2-carboxaldehyde, 1-methyl-, hydrochloride
- 99170-93-1N-Methyl-2-oxazolamine
- 97730-31-9(S)-4'-(2-Methylbutyl)Biphenyl-4-Carbonitrile
- 926293-55-26-Bromo-2-methylpyridine-3-carboxaldehyde
- 95789-13-21,3,7-trimethylpurine-2,6-dione
- 956104-42-02-Bromo-5-nitro-3-(trifluoromethyl)pyridine
- 945683-37-41-butyl-2,3-dimethylimidazolium octanesulfate
- 946052-36-41-Butyl-3-methylpyridinium methanesulfonate
- 942196-38-51-Hexyl-3-methylpyridinium hexafluorophosphat
- 929897-32-51-hexyl-4-methylpridine hexafluorophosphate
| Conditions | Yield |
|---|---|
| In formaldehyde diethyl acetal at 10 - 30℃; for 2.5 - 7.5h; | 91% |
| reaction at -40°C;; |
- 65457-77-4
4-<(1,1'-dimethylbenzyl)oxy>-2-cyclopentenone
A
- 917-54-4
methyllithium
- 99474-57-4, 99474-58-5, 114790-76-0
(1S,4S)-1-Methyl-4-(1-methyl-1-phenyl-ethoxy)-cyclopent-2-enol
| Conditions | Yield |
|---|---|
| In tetrahydrofuran at -30℃; for 1h; | A 86% B 6% |
| Conditions | Yield |
|---|---|
| With n-butyllithium In hexane; dichloromethane at -40 - 20℃; for 1h; Inert atmosphere; | 83% |
| With diethyl ether; lithium | |
| With lithium |
- 109-72-8, 29786-93-4
n-butyllithium
- 3043-52-5
1,2,3,3,4,5-hexamethyl-6-methylene-cyclohexa-1,4-diene
A
- 917-54-4
methyllithium
B
- 75934-66-6
pentamethylpentylbenzene
| Conditions | Yield |
|---|---|
| With N,N,N,N,-tetramethylethylenediamine In Cyclopentane at 55℃; for 5.5h; | A n/a B 77% |
- 3043-52-5
1,2,3,3,4,5-hexamethyl-6-methylene-cyclohexa-1,4-diene
- 594-19-4
tert.-butyl lithium
A
- 917-54-4
methyllithium
B
- 56909-25-2
2,3,4,5,6-pentamethylneopentylbenzene
| Conditions | Yield |
|---|---|
| In cyclohexane at 88℃; for 3.3h; | A n/a B 63% |
| Conditions | Yield |
|---|---|
| With lithium |
| Conditions | Yield |
|---|---|
| With bromobenzene; diethyl ether; lithium | |
| With iodobenzene; diethyl ether; lithium | |
| With lithium |
| Conditions | Yield |
|---|---|
| With Petroleum ether |
- 917-58-8Potassium ethylate
- 917-65-7ALUMINUM METHYL DICHLORIDE
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- 91770-03-5Fatty acids, tall-oil, reaction products with boric acid (H3BO3) and diethanolamine
- 91770-19-3Loquat, ext.
- 91770-40-0Oils, avocado, unsaponifiable fraction
- 91771-33-4Bambusa vulgaris, ext.
- 918511-92-95-Pyridin-3-yl-1H-pyrrolo[2,3-b]pyridine
- 104987-11-3Tacrolimus
- 141-53-7Sodium formate
- 8001-54-5Quaternary ammonium compounds, alkylbenzyldimethyl, chlorides
- 9003-39-8Povidone
- 10161-34-9Trenbolone acetate
- 402957-28-2Telaprevir
- 68-19-9Cyanocobalamin
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Chemistry
This s-block organometallic compound adopts an oligomeric structure both in solution and in the solid state. This highly reactive compound, invariably used as a solution in ethers, is a reagent in organic synthesis as well as organometallic chemistry. Operations involving methyllithium(917-54-4) require anhydrous conditions, because the compound is highly reactive toward water. Oxygen and carbon dioxide are also incompatible with MeLi. Methyllithium(917-54-4) is usually not prepared, but purchased as a solution in various ethers.
The density of methyllithium(917-54-4) is 0.85 g/mL at 20 °C and it has a flash point of 5 °F.
The molecular structure of methyllithium(917-54-4):
Production
2 Li + MeBr → LiMe + LiBr
The lithium bromide forms a complex with the methyllithium(917-54-4). Most commercially available methyllithium(917-54-4) consists of this complex. "Halide-free" methyllithium(917-54-4) is prepared from methyl chloride. Lithium chloride precipitates from the diethyl ether since it does not form a strong complex with methyllithium(917-54-4). The filtrate consists of fairly pure methyllithium(917-54-4).
Safety Profile
Specification
Bonding
These clusters are considered "electron-deficient," that is, they do not follow the octet rule because the molecules lack sufficient electrons to form four 2-centered, 2-electron bonds around each carbon atom, in contrast to most organic compounds. The hexamer is a 30 electron compound (30 valence electrons.) If one allocates 18 electrons for the strong C-H bonds, 12 electrons remain for Li-C and Li-Li bonding. There are six electrons for six metal-metal bonds and one electron per methyl-η3 lithium interaction.
The strength of the C-Li bond has been estimated at around 57 kcal/mol from IR spectroscopic measurements.