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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874622Generated: October 30, 2026

Trimethyl orthoacetate → 5-Methyl-3-(1-methylpyrazol-3-yl)-1,2,4-oxadiazole

https://huagongshe.com/reaction/874622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoacetateHCID 15050—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium ethoxideHCID 2723922—
Reactant1-Methyl-1H-pyrazole-3-carbonitrileHCID 12747510—
CatalystYtterbium triflateHCID 2733225—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product5-Methyl-3-(1-methylpyrazol-3-yl)-1,2,4-oxadiazoleHCID 58487292—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a suspension of hydroxylamine hydrochloride (351 mg, 5.05 mmol) in 4 ml EtOH was added 1.86 ml 21% wt sodium ethoxide in ethanol. The resulting mixture was stirred for 10 min at r.t. before addition of 3-cyano-1-methylpyrazole (70) (535 mg, 5 mmol). The resulting suspension was heated overnight at 90° C. After cooling down, the reaction mixture was diluted with EA then washed with brine. Org. phase was concentrated to dryness to give 506 mg crude intermediate 71. A mixture of the above crude intermediate 71, trifluoromethanesulfonic acid Ytterbium (III) salt (22 mg, 1% mol) and trimethyl orthoacetate (550 μl, 1.2 eq.) in 5 ml EtOH was heated at 85° C. for 2 h. After cooling down to r.t., fine needles formed. After filtration and wash with MeOH 166 mg intermediate 71 was recovered as pale yellow needles. The filtrate was concentrated, subjected to silica gel column purification using 0-100% B (A: hexane; B: EA) to furnish 230 mg 5-methyl-3-(1-methylpyrazol-3-yl)-1,2,4-oxadiazole (72) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980629B2
Source datasetuspto-grants-2015_03
ORD IDord-09db713636db4130a90a5942a5d08f53
Source noteuspto-grants-2015_03