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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681525Generated: November 4, 2026

Methyl iodide → HCID 15037140, compound

https://huagongshe.com/reaction/1681525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantMorpholineHCID 8083—
Reactant3-FuraldehydeHCID 10351—
ReactantChlorotriethylsilaneHCID 13819—
ReactantButyllithiumHCID 178418339—
ReactantCID 53628100HCID 178418400—
SolventTetrahydrofuranHCID 8028—
SolventCyclohexaneHCID 8078—
ProductHCID 15037140HCID 15037140—

Reaction Steps

n-Butyl lithium (a 1.6M solution in THF; 19.0 ml, 30.4 mmol) was added to a solution of morpholine (2.67 ml, 30.4 mmol) in THF (20 ml) at -78 degrees C. under argon. After 20 minutes, 3-furaldehyde (1.8 ml, 28.9 mmol) was added, followed by s-butyl-lithium (a 1.3M solution in cyclohexane; 23.4 ml, 30.4 mmol) after another 20 minutes. Stirring was continued for 2 hours and chlorotriethylsilane (5.1 ml, 30.4 mmol) was added. After 2 hours at -78 degrees C., s Buli (23.4 ml, 30.4 mmol) wad added, followed by iodomethane (5.4 ml, 86.9 mmol) after another 2 hours. The mixture was stirred at room temperature for 15 hours and quenched with ice cold dilute hydrochloric acid. Extraction with ethyl ether and evaporation of the dried (magnesium sulfate) extracts gave an oil, which was purified by flash chromatography on silica using 10% diethyl ether/hexane to give the titled aldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05171863
Source datasetuspto-grants-1992_12
ORD IDord-ba59db5d377949dca20c9fcac35b9dfe
Source noteuspto-grants-1992_12