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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196926Generated: November 1, 2026

Methyl iodide → Lithium diisopropylamide

https://huagongshe.com/reaction/1196926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylamineHCID 7912—
Reactant4-MethylpyridazineHCID 136882—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductLithium diisopropylamideHCID 2724682—
ProductHCID 18956526HCID 18956526—

Reaction Steps

A solution of lithium diisopropylamide was prepared as described in Example 1(i) from diisopropylamine (17.9 g) and n-butyllithium (70.4 ml of a 2.5M solution in hexane) in dry tetrahydrofuran (300 ml) under an atmosphere of dry nitrogen. To this solution at -70° was added 4-methylpyridazine, dropwise with stirring, ensuring that the temperature did not rise above -60°. Iodomethane (27.25 g) was added slowly with stirring, the solution was stirred at -70° for 1 hour and then allowed to warm to room temperature. Water was added and the solution was evaporated to low bulk. The solution was extracted three times with dichloromethane and the combined extracts were dried (Na2SO4) and evaporated. The residue was chromatographed on silica gel using ethyl acetate as eluant. The product fractions were combined and evaporated, and the residual oil was distilled to give the title compound, (10.4 g), b.p. 65°-66° at 0.1 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05116844
Source datasetuspto-grants-1992_05
ORD IDord-ad0863556f3b46e9a840b790fb644b28
Source noteuspto-grants-1992_05