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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270485Generated: October 31, 2026

Methyl iodide → HCID 54519475, compound

https://huagongshe.com/reaction/2270485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
ReactantHCID 54205230HCID 54205230—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54519475HCID 5451947546%

Reaction Conditions

Temperature0 °C

Reaction Steps

N-(2-pyridinylmethoxycarbonyl)-L-leucine methyl ester (490 mg, 1.75 mmol) was dissolved in THF (7.0 mL) and methyl iodide (0.435 ml, 6.99 mmol) was added. The reaction mixture was cooled to 0° C. in a flask protected from moisture. Sodium hydride dispersion (236 mg, 2.62 mmol) was added cautiously and the suspension was sired for 5 hours at room temperature. Ethyl acetate was then added, followed by water, dropwise. The solution was concentrated in vacuo, and the oily residue partitioned between ether and water. The organic layer was washed with sated aqueous NaHCO3 and the combined aqueous extracts acidified to pH 3 with citric acid. The product was extracted with ethyl acetate, the extract was washed with water, 5% aqueous sodium thiosulfate and water, dried (MgSO4), filtered and concentrated. The crude product was purified by column chromatography on silica gel (ethyl acetate/hexane, 3:1) to give a yellow oil (235 mg, 46%). MS (ESI): 295.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06331542B1
Source datasetuspto-grants-2001_12
ORD IDord-4f73a2739e0749a3b7d90a44abb52fe9
Source noteuspto-grants-2001_12