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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375469Generated: October 30, 2026

Sodium Cyanide → Isoquinoline-5-carbonitrile

https://huagongshe.com/reaction/375469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
ReactantIodide IonHCID 30165—
Reactant5-AminoisoquinolineHCID 70766—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 178418260HCID 178418260—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductIsoquinoline-5-carbonitrileHCID 45977062.3%

Reaction Steps

To a cold (0° C.) solution of 10.0 g (61.4 mmol) of 5-aminoisoquinoline in 288 mL of 1.5N hydrochloric acid, was added 15 mL of 5.2M sodium nitrite in water. After approximately 5 minutes, a cool saturated solution of sodium bicarbonate was added to the reaction mixture until the reaction solution tested negative using the iodide and starch paper test. The resultant solution was poured into a cold (0°-5° C.) biphasic mixture containing 300 ml of toluene and 150 mL of an aqueous solution containing 8.4 g (177 mmol) of sodium cyanide and 7.6 g (85 mmol) of copper cyanide. The resultant reaction mixture was warmed to room temperature, reacted for approximately 1 hour, and then diluted with a mixture of ethyl acetate and water. The resulting layers were separated, and the organic phase was dried over sodium sulfate, filtered, and then reduced to dryness under reduced pressure to provide 5.9 g of a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05484926
Source datasetuspto-grants-1996_01
ORD IDord-87ff94b5b52f4b5080079ff642f79dd6
Source noteuspto-grants-1996_01