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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649730Generated: November 2, 2026

Iodoethane → HCID 15137076, compound

https://huagongshe.com/reaction/1649730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium PyrosulfiteHCID 656671—
ReactantHCID 178526763HCID 178526763—
SolventSodium HydroxideHCID 14798—
ProductHCID 15137076HCID 15137076—

Reaction Steps

20.52 g (0.1 mole) of 3-nitro-4-quinoline-thiol are taken up in 150 ml of a molar sodium hydroxide solution. After addition of some sodium pyrosulfite crystals 23.3 g (0.15 mole) of ethyl iodide are added at 60° C. After the reaction has been completed the product formed is extracted with dichloro methane and the extract is evaporated. The 4-ethylthio-3-nitro-quinoline thus obtained (18.6 g) is dissolved in alcohol, an aqueous sodium sulfide solution is added, the reaction mixture is refluxed and then diluted with water. The product is extracted with dichloro methane, the extract is clarified and evaporated. From the residue (13.6 g, yield 83.5%) the hydrochloride is formed by usual methods. Thus 14.0 g of 3-amino-4-ethylthio-quinoline-hydrochloride are obtained. The product is identical with the compound prepared according to Example 1 or 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04921861
Source datasetuspto-grants-1990_05
ORD IDord-3a8fee6f316c444c9bab5f3446105311
Source noteuspto-grants-1990_05