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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292635Generated: November 2, 2026

Pyridine → Ethyl 3-(4-carboxy-2-methylphenylhydrazono)-4-oxopentanoate

https://huagongshe.com/reaction/2292635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Amino-3-methylbenzoic acidHCID 75598—
ReactantEthyl 3-acetyl-4-oxopentanoateHCID 87820—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductEthyl 3-(4-carboxy-2-methylphenylhydrazono)-4-oxopentanoateHCID 86751496—

Reaction Steps

A mixture of 3 g (19.8 mmol) of 4-amino-3-methylbenzoic acid in 50 ml of water and 50 ml of ethanol and 3.56 ml of concentrated hydrochloric acid was cooled in an ice bath and then 1.5 g of NaNO2 (21.8 mmol) in 10 ml of water was added portionwise. The mixture was allowed to come to room temperature and then added to a solution of 4.06 g (21.8 mmol) of ethyl 3-acetyl-4-oxopentanoate and 8 ml of pyridine in 25 ml of ethanol. The reaction mixture was left for 24 hr at room temperature with stirring. The mixture was acidified with concentrated hydrochloric acid and the mixture diluted with 20 ml of water. The resulting solid was collected and washed with water and pentane to yield 5.2 g of ethyl 3-(4-carboxy-2-methylphenylhydrazono)-4-oxopentanoate with m.p. 161°-162.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05684024
Source datasetuspto-grants-1997_11
ORD IDord-c00576b04f1c4997b885d644cc60d1bd
Source noteuspto-grants-1997_11