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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204901Generated: October 31, 2026

Potassium Iodide → HCID 71272497, compound

https://huagongshe.com/reaction/2204901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Hydroxybenzyl cyanideHCID 26548—
Reactant1-Octanol, 8-chloro-HCID 90012—
SolventDimethylformamideHCID 6228—
ProductHCID 71272497HCID 7127249762.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

20.0 g (150 mmol) of (4-hydroxyphenyl)acetonitrile and 29.5 g (179 mmol) of 8-chlorooctan-1-ol are dissolved in 400 mL of N,N-dimethylformamide. 41.5 g (300 mmol) of potassium carbonate and 5.0 g (30 mmol) of potassium iodide are added and the suspension is heated to 80° C. After 48 h, the excess of potassium carbonate is filtered off and the resulting filtrate is poured to icy water. The aqueous layer is extracted twice with ethyl acetate. Combined organic layers are washed with brine and evaporated to dryness. The crude is purified twice on column chromatography (SiO2, Heptane/ethyl acetate: 7/3) and dried overnight at 40° C. 24.5 g of {4-[(8-hydroxyoctyl)oxy]phenyl}acetonitrile are obtained as a yellow solid (62% yield). This material proves chromatographically homogenous and displays spectral characteristics consistent with its assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09366906B2
Source datasetuspto-grants-2016_06
ORD IDord-9902c0f1977044d1b298d87435721eeb
Source noteuspto-grants-2016_06