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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437589Generated: October 30, 2026

Iodoethane → HCID 21428663, compound

https://huagongshe.com/reaction/437589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodiumHCID 5360545—
ReactantHCID 21428671HCID 21428671—
SolventEthanolHCID 702—
ProductHCID 21428663HCID 21428663—

Reaction Steps

1.3 gm of N-[3-(3,4-dihydro-4,4-dimethyl-7-hydroxy-1,3-dioxo-2(1H)-isoquinolyl)-propyl]-N-[3-(3,4-dihydro-4,4-dimethyl-1,3-dioxo-2(1H)-isoquinolyl)-propyl]-methylamine were dissolved in 10 ml of absolute ethanol, the resulting solution was added to a solution of 0.06 gm of sodium in 10 ml of absolute ethanol, and 0.42 gm of ethyl iodide was added to the mixed solution. The mixture was refluxed for 30 minutes, another 0.42 gm of ethyl iodide was added, and the mixture was refluxed again for 30 minutes. The product was purified on a silicagel column (eluant: chloroform/ethanol = 25:1), and the hydrochloride was precipitated from acetone with ethereal hydrochloric acid. The hydrochloride sintered above 45° C; yield: 0.5 gm (35% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031219
Source datasetuspto-grants-1977_06
ORD IDord-250868536a51468cb0b3dcbfa2dc3538
Source noteuspto-grants-1977_06