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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1590570Generated: November 1, 2026

Cyanogen Bromide → HCID 21459520, compound

https://huagongshe.com/reaction/1590570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantHCID 10471741HCID 10471741—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21459520HCID 2145952074.4%

Reaction Steps

Potassium t-butoxide (614 mg, 5.74 mmol) is added in portions at room temperature to a solution of 2,4,5-tribromopyrrole-3-carbonitrile (1.50 g, 4.56 mmol) in anhydrous tetrahydrofuran (20 mL). After 15 minutes a solution of cyanogen bromide (177 mg, 5.74 mmol) in tetrahydrofuran (5 mL) is added dropwise. The reaction solution is stirred at room temperature overnight as it turns cloudy. The mixture is diluted with water and extracted with ethyl acetate. The organic layer is washed with water and saturated sodium chloride and dried over (Na2SO4). Evaporation of the solvent and crystallization of the residue from ether gives a white solid (1.20 g); mp 195.0°-197.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05204332
Source datasetuspto-grants-1993_04
ORD IDord-c85536bb4039441ba1f37fc9e7bba3f0
Source noteuspto-grants-1993_04