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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159185Generated: November 2, 2026

Cyanogen Bromide → HCID 178482987, compound

https://huagongshe.com/reaction/1159185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 68644158HCID 68644158—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178482987HCID 17848298728%

Reaction Steps

N1-(3-Chloro-phenyl)-N1-methyl-propane-1,2,3-triamine (0.321 g, 1.5 mmol) was dissolved in tetrahydrofurane (5 ml) and potassium carbonate (0.249 g, 1.8 mmol) was added. Under cooling with an ice-bath a solution of cyanogen bromide (0.191 g, 1.8 mmol) in tetrahydrofurane (5 ml) was added dropwise. The cooling bath was removed and stirring was continued for one hour. Ethyl acetate (50 ml) and water (20 ml) were added and the organic layer was separated. The mixture was extracted again with ethyl acetate. The combined organic layers were dried over magnesium sulfate and evaporated. The residue was recrystallised from ethyl acetate to yield 0.1 g (28%) of a white solid; MS (ISP): 239.2 ((M+H)+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812047B2
Source datasetuspto-grants-2010_10
ORD IDord-68896c109084470bb7632addfe745cd0
Source noteuspto-grants-2010_10