Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727839Generated: October 29, 2026

Water → 5-(2,6-difluorobenzyl)-4-methyl-4H-1,2,4-triazole-3-carboxamide

https://huagongshe.com/reaction/727839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CyanideHCID 8929—
Reactant5-(2,6-difluorobenzyl)-3-hydroxymethyl-4-methyl-4H-1,2,4-triazoleHCID 19904233—
CatalystHCID 178418406HCID 178418406—
SolventTolueneHCID 1140—
Product5-(2,6-difluorobenzyl)-4-methyl-4H-1,2,4-triazole-3-carboxamideHCID 19904235—

Reaction Steps

1.43 g (6 mmol) of 5-(2,6-difluorobenzyl)-3-hydroxymethyl-4-methyl-4H-1,2,4-triazole and 5.22 g (60 mmol) of manganese dioxide are heated under reflux in 40 ml of toluene for 3 hours using a water separator. The reaction mixture is then cooled and filtered over Hyflo, and the filtrate is concentrated by evaporation. The residue is added to 90 ml of isopropanol saturated with ammonia. At 0°, 1.47 g (30 mmol) of sodium cyanide and 10.44 g (120 mmol) of manganese dioxide are added. The reaction mixture is stirred for 4 hours at 0° and filtered over Hyflo. The filtrate is concentrated by evaporation. Recrystallisation of the residue from ethanol yields the pure 5-(2,6-difluorobenzyl)-4-methyl-4H-1,2,4-triazole-3-carboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05045556
Source datasetuspto-grants-1991_09
ORD IDord-f942d85ed94c4f01b99c0feca55ffa61
Source noteuspto-grants-1991_09