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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275422Generated: October 30, 2026

Sodium Cyanide → (4-Phenoxynaphthalen-1-yl)acetonitrile

https://huagongshe.com/reaction/1275422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
ReactantHCID 22119575HCID 22119575—
SolventDimethyl SulfoxideHCID 679—
Product(4-Phenoxynaphthalen-1-yl)acetonitrileHCID 1673677649%

Reaction Conditions

Temperature50 °C

Reaction Steps

Sodium cyanide (3.7 g; 75 mMol) was dissolved in DMSO (50 mL, dried over molecular sieves). The mixture was heated in an oil bath maintained at 50° C., and 15.7 g (50 mMol) of 1-bromomethyl-4-phenoxynaphthalene, prepared as described above, in 75 mL of DMSO was added dropwise. After addition was complete, stirring was continued for 0.5 hours. The temperature was raised to 70° C., and stirring was continued for 1.0 hour. The oil bath was turned off, and the stirring was continued overnight. The mixture was poured onto ice, and extracted with ether. The combined organic extractions were washed with brine and dried over magnesium sulfate. The product was obtained as a white, crystalline solid (6.24 g; 49% yield). mass 259. A sample was purified for analysis by medium pressure chromatography on silica gel, eluting with ethyl acetate:hexane/1:9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06160175
Source datasetuspto-grants-2000_12
ORD IDord-bcd05489d9a6498b9a41efe12a9cdefe
Source noteuspto-grants-2000_12