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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41254Generated: October 30, 2026

Sodium Hydroxide → ethyl 2-(5-chloro-4-formyl-3-methyl-1H-pyrazol-1-yl)acetate

https://huagongshe.com/reaction/41254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl (3-methyl-5-oxo-4,5-dihydro-1H-pyrazol-1-yl)acetateHCID 5085836—
SolventDimethylformamideHCID 6228—
Productethyl 2-(5-chloro-4-formyl-3-methyl-1H-pyrazol-1-yl)acetateHCID 737985—

Reaction Steps

DMF (2.01 mL) was cooled to 0° C. and phosphorus oxychloride (5.67 mL, 60.8 mmol) was added dropwise. This reaction mixture was warmed to room temperature, and then ethyl(3-methyl-5-oxo-4,5-dihydro-1H-pyrazol-1-yl)acetate (1.60 g, 8.69 mmol) was added slowly, and then the mixture was stirred at 110° C. for 3.5 hours. After the reaction was completed, the mixture was poured into ice water, a 5N aqueous solution of sodium hydroxide and sodium hydrogencarbonate were added to the mixture for neutralization. The extraction with ethyl acetate was carried out, the organic layer was washed with brine and dried over anhydrous magnesium sulfate. The mixture was filtered to obtain filtrate, and the solvent was distilled off under reduced pressure to yield a solid, and the obtained solid was washed with n-heptane/diisopropyl ether mixture (1:1), and dried to obtain the title compound 1.28 g (5.55 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530504B2
Source datasetuspto-grants-2013_09
ORD IDord-bfbca67e1b934f51b487cd30b7391922
Source noteuspto-grants-2013_09