Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262514Generated: November 4, 2026

Allyl bromide → HCID 10773123, compound

https://huagongshe.com/reaction/2262514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178510443HCID 178510443—
SolventDimethylformamideHCID 6228—
ProductHCID 10773123HCID 1077312340%

Reaction Conditions

Temperature80 °C

Reaction Steps

3-Amino-4-pyrazolecarbonitrile 1 (Acros, 1.08 g, 10.0 mmol), allylbromide (Acros, 1.45 g, 12 mmol) and anhydrous potassium carbonate (Fisher, 1.65 g, 12 mmol) were suspended in 10 mL anhydrous DMF and heated at 80° C. under argon overnight. The solution was concentrated. Water was added (100 mL) and the organics were extracted with dichloromethane (3×100 mL). The combined dichloromethane fractions were washed with water (50 mL) and brine (50 mL) and were dried (magnesium sulfate). Concentration of the organics afforded a solid which was subjected to flash chromatography on silica gel (gradient elution 2:1 to 3:2 hexane: ethyl acetate). 589 mg (40%) of a white solid was obtained which was seen by NMR to contain an inseparable mixture of 5 and 6 in a 2.1:1 ratio. This mixture was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851468B2
Source datasetuspto-grants-2010_12
ORD IDord-106de23393f9449a959ca2eacfd8058e
Source noteuspto-grants-2010_12