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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231657Generated: November 1, 2026

Methanol → 1-(4-Amino-3-formyl-5-methylphenyl)-1,2,4-triazole

https://huagongshe.com/reaction/2231657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantHydrideHCID 166653—
Reactant1-(4-Amino-3-cyano-5-methylphenyl)-1,2,4-triazoleHCID 21285532—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Amino-3-formyl-5-methylphenyl)-1,2,4-triazoleHCID 21285533—

Reaction Steps

Diisobutylalumnium hydride (11.1 cm3 of a 1.5M solution in toluene) was added dropwise at 0° to a stirred suspension of 1-(4-amino-3-cyano-5-methylphenyl)-1,2,4-triazole (15 g) in THF (20 cm3). The solution was stirred at room temperature for 0.5 hours, heated under reflux for 2 hours, cooled, and treated with methanol (1 cm3) and water (100 cm3). Solid material was filtered off and washed with methanol (50 cm3) and the filtrate was evaporated in vacuo. The residue was taken into 2M hydrochloric acid (20 cm3), warmed for 10 minutes at 100° , and cooled. The solution was neutralised with saturated aqueous sodium carbonate solution and extracted with chloroform (4×50 cm3). The combined organic extracts were dried (MgSO4) and evaporated to give an oil which was chromatographed on silica (Merck "MK 60.9385" [Trade Mark]) eluting with ethyl acetate. Combination and evaporation of appropriate fractions followed by recrystallisation from ethyl acetate/hexan afforded the title compound, m.p. 209°-211° (1.27 g), characterised by n.m.r. and i.r. spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04783467
Source datasetuspto-grants-1988_11
ORD IDord-c9d54438cab148b180a59178d1d36c0f
Source noteuspto-grants-1988_11