Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822889Generated: October 30, 2026

Cyanogen Bromide → 4-[(5-Amino-1,3,4-oxadiazol-2-yl)methyl]phenol

https://huagongshe.com/reaction/1822889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
Reactant2-(4-Hydroxyphenyl)acetohydrazideHCID 3731866—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product4-[(5-Amino-1,3,4-oxadiazol-2-yl)methyl]phenolHCID 21919315—

Reaction Conditions

Temperature2.5 °C

Reaction Steps

Solid BrCN 6.059 g (57.2 mmol) was added in one portion into ice-cooled slurry of (4-hydroxy-phenyl)-acetic acid hydrazide 8.642 g (52.0 mmol) and KHCO3 6.510 g (65 mmol) in MeOH (100 mL). The mixture was stirred at 0-5° C. for 1 hour, the ice bath allowed to melt and stirred at room temperature overnight (18 hr). The reaction mixture was diluted with water (100 mL), stirred for 1 hour, the precipitate was collected by filtration, washed with water and dried on high vacuum. A second fraction precipitated after concentrating and cooling the supernatants.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07037909B2
Source datasetuspto-grants-2006_05
ORD IDord-7b2aa49c5bc340b087a376f9edc1fc9b
Source noteuspto-grants-2006_05