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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858735Generated: October 26, 2026

Acetylacetone → (5,7-Dimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)methanol

https://huagongshe.com/reaction/858735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetylacetoneHCID 31261—
ReactantHCID 178508532HCID 178508532—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
Product(5,7-Dimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)methanolHCID 44141733—

Reaction Conditions

Temperature5 °C

Reaction Steps

The title compound was prepared by a slight modification of a reported procedure (Lippman, E.; Becker, V., Z. Chem., 1974, 14, 405): A solution of (5-amino-1H-1,2,4-triazol-3-yl)methanol glycolate (30.7 g, 0.161 mol, from Step 1, above) and 2,4-pentadione (32.3 g, 0.323 mol, 2 equiv) in a mixture of EtOH (750 mL) and AcOH (250 mL) was refluxed 20 h. At the beginning the reaction mixture was clear solution, then gradually turned yellow towards the end of the heating period. The solvent was removed under reduced pressure, and the resulting yellow paste triturated with EtOH (100 mL) and stirred for 15 min. The slurry was chilled to 5° C. (ice bath) with stirring for 30 min, filtered, and washed with cold (0–5° C.) EtOH. The product was dried in vacuo at 25–30° C. to give 24 g (83.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148226B2
Source datasetuspto-grants-2006_12
ORD IDord-16bb9c84b1d742c2b62c61be9309e337
Source noteuspto-grants-2006_12