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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1629222Generated: November 1, 2026

Ammonium Chloride → 1-(1-Isopropyl-1H-1,2,4-triazol-5-YL)ethanone

https://huagongshe.com/reaction/1629222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantDimethylacetamideHCID 31374—
Reactant1-(propan-2-yl)-1H-1,2,4-triazoleHCID 12762443—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-(1-Isopropyl-1H-1,2,4-triazol-5-YL)ethanoneHCID 1497833987%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1-isopropyl-1H-[1,2,4]triazole (33 g, 300 mmol) in THF at −10° C. was added n-butyllithium (145 mL, 2.5M, 360 mmol) dropwise over 45 min, and then the mixture stirred at 0° C. for 30 min. DMA (35 mL) was added, the mixture allowed to warm to RT and stirred for 1 h. The resultant suspension was treated with saturated aqueous ammonium chloride (300 mL). The aqueous phase was extracted with ethyl acetate and the combined organic extracts dried (Na2SO4), filtered and concentrated in vacuo to give 1-(2-Isopropyl-2H-[1,2,4]triazol-3-yl)-ethanone as a pale orange oil (40.1 g, 87%). 1H NMR δ (ppm)(CDCl3): 7.93 (1 H, s), 5.58-5.46 (1 H, m), 2.72 (3 H, d, J=0.78 Hz), 1.49 (6 H, dd, J=6.61, 0.78 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785626B2
Source datasetuspto-grants-2014_07
ORD IDord-93fbfcea144142f886bb54d890731896
Source noteuspto-grants-2014_07