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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204911Generated: November 2, 2026

Potassium Iodide → HCID 71272057, compound

https://huagongshe.com/reaction/2204911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant11-Bromo-1-undecanolHCID 74163—
Reactant4-Hydroxy-3-methoxyphenylacetonitrileHCID 78220—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 71272057HCID 7127205774.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

11.0 g (67 mmol) of [4-hydroxy-3-methoxy-phenyl]acetonitrile and 20.4 g (81 mmol) of 11-bromoundecan-1-ol were dissolved in 100 mL of N,N-dimethylformamide. 18.7 g (135 mmol) of potassium carbonate and 2.2.0 g (13 mmol) of potassium iodide were added and the suspension was heated to 80° C. After 48 h, the reaction mixture was cooled to room temperature and 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. 16.6 g of {4-[(11-hydroxyundecyl)oxy]-3-methoxyphenyl}acetonitrile are obtained as a yellow solid (74% 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-bee75a19424f46a7b9e314e57660401f
Source noteuspto-grants-2016_06