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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209561Generated: October 27, 2026

Cyanogen Bromide → 4,5-Dichloro-2-(3,4-dichlorophenyl)pyrrole-1,3-dicarbonitrile

https://huagongshe.com/reaction/2209561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
Reactant4,5-dichloro-2-(3,4-dichlorophenyl)-1H-pyrrole-3-carbonitrileHCID 183555—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product4,5-Dichloro-2-(3,4-dichlorophenyl)pyrrole-1,3-dicarbonitrileHCID 1501015664.7%

Reaction Steps

Potassium t-butoxide (617 mg, 55 mmol) is added in portions to a solution of 3-cyano-4,5-dichloro 2-(3,4-dichlorophenyl)pyrrole (1.52 g, 5 mmol ) in anhydrous THF (20 mL). After 30 minutes, a solution of cyanogen bromide (583 mg, 5.5 mmol) in THF (1 mL) is added. The reaction mixture is stored at room temperature overnight. The solvent is removed in a rotary evaporator. The residue is treated with water and extracted witch ethyl acetate. The organic layer is washed with water and saturated sodium chloride and dried (MgSO4). Evaporation and crystallization of the residue from ethyl acetate gives while crystals (1.07 g); mp 250.5°-252.0° C.; IR (nujol) 2255, 2245 cm-1 (CN) 13C NMR (DMSO-d6) 102.7 (N-CN), 113.7 (3-CN); Mass spectrum 331.9 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05455263
Source datasetuspto-grants-1995_10
ORD IDord-8117eb166e214ae79272083d1b629f62
Source noteuspto-grants-1995_10