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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296983Generated: October 30, 2026

Water → 4-(3-formylbenzyl)-5-methoxy-2,4-dihydro-3H-1,2,4-triazol-3-one

https://huagongshe.com/reaction/2296983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(Bromomethyl)benzaldehydeHCID 7127825—
Reactant3H-1,2,4-Triazol-3-one, 1,2-dihydro-5-methoxy-HCID 135499741—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product4-(3-formylbenzyl)-5-methoxy-2,4-dihydro-3H-1,2,4-triazol-3-oneHCID 1838886718.8%

Reaction Steps

To a solution of 0.92 g (8.0 mmol) of 5-methoxy-2,4-dihydro-3H-1,2,4-triazol-3-one in 15 ml of dry acetonitrile was added 1.16 g (8.4 mmol) of potassium carbonate. To the mixture was added dropwise a solution of 1.59 g of crude 3-(bromomethyl)benzaldehyde in 30 ml of dry acetonitrile at 55° C. under an atmosphere of nitrogen. After the mixture was stirred at the same temperature for additional 6 hours, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, dried and concentrated. The residue (1.31 g) was subjected to silica gel column chromatography (eluted with n-hexane:ethyl acetate=1:1 and then 1:2) to obtain 0.35 g (1.50 mmol) of 4-(3-formylbenzyl)-5-methoxy-2,4-dihydro-3H-1,2,4-triazol-3-one as white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06489487B1
Source datasetuspto-grants-2002_12
ORD IDord-cf55b95f9ccd4d0f95c8cea049ec55de
Source noteuspto-grants-2002_12