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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770255Generated: November 1, 2026

Cyanogen Bromide → HCID 57286927, compound

https://huagongshe.com/reaction/1770255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantSodium HydroxideHCID 14798—
Reactant1,2-Ethanediamine, N,N'-bis(2-methylphenyl)-HCID 66759—
SolventEthanolHCID 702—
ProductHCID 57286927HCID 5728692792.6%

Reaction Steps

N,N' Bistolyl ethylene diamine (105.8 mg, .44 mmol) was taken up in EtOH (3 mL) to provide a light purple solution. This solution was then placed in a one-necked round-bottom flask (25 mL) equipped with magnetic stirbar and reflux condenser. To this solution, cyanogen bromide (50 mg, 0.47 mmol) in ethanol (2 mL) was added in a single portion. The resultant reaction mixture was stirred for 1 h. It was noted that the solution turned clear. The solution was then brought to reflux and maintained at that temperature for 16 h. The reflux condenser was then removed, allowing the solvent to evaporate. The reaction mixture was then fused at 150° C. for 30 min to provide a brown solid. This solid was immediately taken up in ethanol (4 mL) and placed into a centrifuge tube. To this solution 1N NaOH was added (8 mL) to provide a "whispy" tan precipitate. After several failed attempts to pellet the precipitate, the solution was simply extracted with chloroform (20 mL). The chloroform was concentrated to dryness to provide a clear oil (108.1 mg, 92.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05385946
Source datasetuspto-grants-1995_01
ORD IDord-ac4596bbeda64305b7263b3df06ac343
Source noteuspto-grants-1995_01