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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696183Generated: October 31, 2026

Potassium Cyanide → 4-Aminothiane-4-carbonitrile

https://huagongshe.com/reaction/1696183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium ChlorideHCID 25517—
ReactantTetrahydrothiopyran-4-oneHCID 66173—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product4-Aminothiane-4-carbonitrileHCID 15818740111.2%

Reaction Steps

To a solution of potassium cyanide (5.6 g) and ammonium chloride (5.06 g) in water (17 mL) was added a solution of tetrahydro-4H-thiopyran-4-one (10 g) in methanol (22 mL), and the mixture was refluxed under heating overnight. After cooling to room temperature, to the reaction mixture was added an aqueous 1N sodium hydroxide solution, and the mixture was extracted with diethylether. The organic layer was dried over magnesium sulfate and filtered. The filtrate was concentrated in vacuo, and to a solution of the resultant residue in diethylether was added a solution of 4N hydrochloric acid in ethyl acetate. The precipitates were collected by filtration to give 4-amino-tetrahydrothiopyran-4-carbonitrile (13.6 g, yield: 88%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163759B2
Source datasetuspto-grants-2012_04
ORD IDord-8d7f56609bc84c3bb8f4d21d6f06b8ac
Source noteuspto-grants-2012_04