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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249047Generated: November 1, 2026

Sodium Iodide → 2-Bromobenzene-1-carbonyl cyanide

https://huagongshe.com/reaction/2249047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantAcetonitrileHCID 6342—
Reactant2-Bromobenzoyl chlorideHCID 23542—
Product2-Bromobenzene-1-carbonyl cyanideHCID 12969202—

Reaction Steps

The reaction was carried out under Argon. Cuprous cyanide (6.52q, 72.8 mmol) and anhydrous sodium iodide (20.25g, 135 mmol) were stirred for 2 minutes in anhydrous acetonitrile (100 ml). The resulting solution was mixed with o-bromo benzoyl chloride (15.0q, 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 (7.14q, 50%), meltinq point 64° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05041681
Source datasetuspto-grants-1991_08
ORD IDord-5b92836972654527aa4eff5e4079828f
Source noteuspto-grants-1991_08