Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459403Generated: October 31, 2026

Iodoethane → HCID 53664223, compound

https://huagongshe.com/reaction/1459403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
ReactantHCID 53924158HCID 53924158—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53664223HCID 5366422343.8%

Reaction Steps

To a well-stirred suspension of N-adamantan-1-yl-2-hydroxymethyl-3-pyridin4-yl-2-pyridin-4-ylmethyl-propionamide (40 mg, 0.1 mmol) in anhydrous tetrahydrofuran (0.50 ml), sodium hydride (7.8 mg of 60% mineral oil dispersion; 0.2 mmol of sodium hydride) was added. After stirring at ambient temperature for 15 minutes, ethyl iodide (15.8 μl, 0.20 mmol) was added. After stirring for 2 hours at ambient temperature, the reaction was quenched by the addition of dilute aqueous sodium bicarbonate/methylene chloride (10 ml of each). The mixture was then extracted with three 10 ml portions of methylene chloride. The combined organic extracts were dried (anhydrous sodium sulfate), and concentrated in vacuo to an oil (54 mg). Flash chromatography (silica gel, 40 micron mesh; elution with methanol/ethyl acetate=1:9 in volume) afforded the title compound (free base) (19 mg) as an amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05854232
Source datasetuspto-grants-1998_12
ORD IDord-4d7dd5e2e3c144d0b54ec211f16e12b7
Source noteuspto-grants-1998_12