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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371574Generated: November 1, 2026

Methyl iodide → 5183-61-9

https://huagongshe.com/reaction/1371574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 2-oxocyclohexanecarboxylateHCID 95543—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product5183-61-9HCID 12368134—

Reaction Conditions

Temperature5 °C

Reaction Steps

To a suspension of sodium hydride (5.0 g, 0.125 mol) in tetrahydrofuran (250 mL) was added a solution of ethyl 2-oxocyclohexanecarboxylate (19.9 mL, 0.125 mol) in tetrahydrofuran (30 mL) whilst maintaining the temperature of the mixture between 10° C. and 15° C. by means of an ice bath. After stirring at 5° C. for 1 hour, butyl lithium (52.5 mL, 2.5 M solution in hexanes, 131 mmol) was added dropwise while maintaining the temperature below 12° C. After stirring at 5° C. for 30 minutes, iodomethane (7.8 mL, 125 mmol) was added. The reaction mixture was stirred at 5° C. for 1.5 hours and then quenched with a saturated solution of ammonium chloride. The mixture was diluted with ethyl ether, washed with water. The organic extracts were dried over magnesium sulfate and concentrated. The resulting residue was distilled (100–110° C., 0.1 torr) to obtain the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157475B2
Source datasetuspto-grants-2007_01
ORD IDord-2afc76b8c8a04ac2b47c2c5bd71a3bee
Source noteuspto-grants-2007_01