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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646754Generated: October 30, 2026

Methyl iodide → HCID 10375132, compound

https://huagongshe.com/reaction/1646754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylamineHCID 7912—
ReactantTetrahydrofuranHCID 8028—
Reactant1H-IndoleacetonitrileHCID 169731—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
ProductHCID 10375132HCID 10375132—

Reaction Steps

To a solution of diisopropylamine (809 mg) in tetrahydrofuran (20 ml) at -30° C. under nitrogen atmosphere was added 1.64M butyllithium in hexane (5.33 ml). After being stirred at the same temperature for 30 minutes, the mixture was treated with a solution of indol-2-yl-acetonitrile (1.25 g) in tetrahydrofuran (10 ml) at -60° C. over 15 minutes. The mixture was stirred at the same temperature for an hour, and a solution of methyl iodide (1.14 g) in tetrahydrofuran (10 ml) was added dropwise over an hour. After the mixture was stirred at -60° C. for one hour and at ambient temperature for 2 hours, it was diluted with chilled water, and extracted two times with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was purified by alumina column chromatography (10% ethylacetate-toluene) to give 2-(indol-2-yl)-2-methylpropiononitrile (354 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05180728
Source datasetuspto-grants-1993_01
ORD IDord-a902f114a47d4aa7b26f1a74da4fda63
Source noteuspto-grants-1993_01