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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221548Generated: October 26, 2026

Benzaldehyde → HCID 178469784, compound

https://huagongshe.com/reaction/2221548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl (ethoxymethylene)malonateHCID 6871—
ReactantHydrazine, ethyl-, ethanedioate (1:1)HCID 96181—
ReactantSodium BicarbonateHCID 516892—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178469784HCID 17846978428%

Reaction Steps

A mixture of ethylhydrazine oxalate (5.0 g), sodium hydrogen carbonate (5.60 g), water (10 mL) and ethanol (50 mL) was stirred at room temperature for 15 min. Benzaldehyde (3.53 g) was added to the reaction mixture, and the mixture was further stirred at room temperature for 1 hr. To the reaction mixture was added diethyl ethoxymethylenemalonate (7.91 g), and the mixture was heated under reflux for 2 hrs. The reaction mixture was cooled to room temperature, concentrated hydrochloric acid (3 mL) was added and the mixture was further heated under reflux for 15 hrs. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated to give ethyl 1-ethyl-3-hydroxy-1H-pyrazole-4-carboxylate as pale-yellow crystals (1.72 g, yield 28%). The crystals were recrystallized from ethyl acetate-hexane. melting point: 109-110° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368578B2
Source datasetuspto-grants-2008_05
ORD IDord-60e2addb09e44508b5da6a9aad86a4c0
Source noteuspto-grants-2008_05