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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248652Generated: October 29, 2026

Sodium Iodide → 2-Bromobenzene-1-carbonyl cyanide

https://huagongshe.com/reaction/248652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantAcetonitrileHCID 6342—
Reactant2-Bromobenzoyl chlorideHCID 23542—
Product2-Bromobenzene-1-carbonyl cyanideHCID 1296920250%

Reaction Steps

The reaction was carried out under Argon. Cuprous cyanide (6.52 g, 72.8 mmol) and anhydrous sodium iodide (20.25 g, 135 mmol) were stirred for 2 minutes in anhydrous acetonitrile (100 ml). The resulting solution was mixed with o-bromo benzoyl chloride (15.0 g, 68 mmol) whereupon an orange precipitate formed. The mixture was stirred for 30 minutes at room temperature, filtered and concentrated in vacuo. The residue was taken up in dichloromethane and the resulting precipitate was filtered off. Concentration of the filtrate under reduced pressure gave a yellow solid. Recrystallisation from 60°-80° C. b.p.t. petroleum ether afforded o-bromo benzoyl cyanide as yellow crystals (7.14 g, 50%), melting point 64° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05210312
Source datasetuspto-grants-1993_05
ORD IDord-9a11406d8d2f473788db22b1f38ae61f
Source noteuspto-grants-1993_05