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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825361Generated: November 3, 2026

Ammonium Chloride → 1-(5-Ethyl-1-methyl-1H-pyrazol-3-yl)ethanone

https://huagongshe.com/reaction/1825361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantN-Methoxy-N-methyl-5-ethyl-1-methylpyrazole-3-carboxamideHCID 19967595—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product1-(5-Ethyl-1-methyl-1H-pyrazol-3-yl)ethanoneHCID 22145403—

Reaction Conditions

Temperature0 °C

Reaction Steps

N-Methoxy-N-methyl-5ethyl-1-methylpyrazole-3-carboxamide (2.9 g) in dry tetrahydrofuran (100 ml), under argon was cooled to −20° C. and treated with methylmagnesium bromide (9.8 ml of a 3M solution in ether). A precipitate was initially formed that re-dissolved on complete addition. The reaction mixture was stirred at 0° C. for 2 h. and then poured into saturated ammonium chloride. The aqueous phase was extracted with ethyl acetate and the combined organic phases washed with brine, dried over anhydrous magnesium sulphate and concentrated to a brown oil. The crude product was purified by silica gel chromatography eluting with 50% ethyl acetate/hexane to give the title compound as a pale brown oil. (1.97 g, 88%); (Found: M+, 152.0950. C8H12N2O requires M 152.0950); nmax (CH2Cl2) 1693, 1472, 1376 and 1352 cm−1; dH(CDCl3) 1.28 (3H, t, J7.4 Hz), 2.54 (3H, s), 2.61 (2H, q, J7.4 Hz), 3.84 (3H, s) and 6.56 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045619B2
Source datasetuspto-grants-2006_05
ORD IDord-66611af716db41169d9c186f28c85082
Source noteuspto-grants-2006_05