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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211183Generated: October 31, 2026

Cyanogen Bromide → HCID 14951345, compound

https://huagongshe.com/reaction/2211183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantSodium BicarbonateHCID 516892—
Reactant2-[(3-Trifluoromethylphenyl)amino]benzoic acid hydrazideHCID 13167827—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 14951345HCID 1495134569%

Reaction Steps

To a room temperature solution of 2-[(3-trifluoromethylphenyl)amino]benzoic acid hydrazide (532.7 mg, 1.81 mmoles) in 5 ml of dioxane is added sodium bicarbonate (155.0 mg, 1.84 mmoles) in 5 ml of water. After stirring at room temperature for five minutes, cyanogen bromide (192.0 mg, 1.81 mmoles) is added, and stirring is continued for 2.5 hours. The tan precipitate is removed by filtration and washed with 10 ml of 50% aqueous dioxane. Drying in vacuo provides 398.0 mg (69%) of 5-[2-[[3-(trifluoromethyl)phenyl]amino]phenyl]-1,3,4-oxadiazol-2-amine, mp 185°-187° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05462952
Source datasetuspto-grants-1995_10
ORD IDord-8f741bdf79d542c8a3b122b598a485b9
Source noteuspto-grants-1995_10