Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589126Generated: November 4, 2026

Potassium Cyanide → HCID 73180951, compound

https://huagongshe.com/reaction/1589126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
ReactantChlorineHCID 24526—
ReactantHCID 86106740HCID 86106740—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 73180951HCID 7318095174%

Reaction Steps

7.8 g of chlorine were passed into a cooled solution of 12.9 g of 2-formyltetrahydropyran oxime in 140 ml of ether at below 0° C. Thereafter, the volatile constituents of the reaction mixture were stripped off, the residue was taken up in 200 ml of methylene chloride, and the mixture was kept at room temperature for 24 hours. This liquid was then added dropwise to a suspension, cooled to 10°-15° C., of 6.8 g of potassium cyanide in 75 ml of methanol, and the mixture was stirred for a further 3 hours at room temperature. The precipitated potassium chloride was filtered off under suction, the filtrate was evaporated down, the residue was taken up in ether, the solution was washed three times with water and dried over magnesium sulfate, and the solvent was stripped off under 0.005 mbar and at 30° C. to give 11.3 g of α-oximino(tetrahydropyran-2-yl)-acetonitrile as a yellowish solid which melted from 45° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04568668
Source datasetuspto-grants-1986_02
ORD IDord-c00b37eb73a54a349278299f7d2a347d
Source noteuspto-grants-1986_02