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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082273Generated: October 26, 2026

Sodium Iodide → 2,3-Dicyanonaphthalene

https://huagongshe.com/reaction/2082273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant1,2-Bis(dibromomethyl)benzeneHCID 83234—
ReactantFumaronitrileHCID 637930—
ReactantSodium BisulfiteHCID 23665763—
SolventDimethylformamideHCID 6228—
Product2,3-DicyanonaphthaleneHCID 60127073%

Reaction Conditions

Temperature75 °C

Reaction Steps

One hundred grams (0.67 mole) of sodium iodide was added to a well-stirred solution of 42.2 g (0.1 mole) of α,α,α',α'-tetrabromo-o-xylene and 13.5 g (0.173 mole) of fumaronitrile in 400 ml of anhydrous N,N-dimethylformamide, and the resulting mixture was stirred at 75° C. for about 7 hours in an atmosphere of nitrogen. After the reaction, the mixture was poured into about 2 kg of ice, and thereto was slowly added sodium hydrogen sulfite until the red-brown colored aqueous solution turned to light yellow. After adding a slightly excessive quantity of sodium hydrogen sulfite, the resulting mixture was stirred for a while and then allowed to stand overnight at room temperature. The deposited light yellow-colored solid product was collected by filtration with suction, thoroughly washed with water, and allowed to dry. The light yellow-colored solid product thus obtained was recrystallized from ethanol/chloroform mixture to obtain 13 g (73%) of 2,3-dicyanonaphthalene as a colorless crystalline material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05188922
Source datasetuspto-grants-1993_02
ORD IDord-1e55558865f74cd4952cee46b45e521f
Source noteuspto-grants-1993_02