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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182506Generated: November 2, 2026

Benzoylhydrazine → HCID 10198473, compound

https://huagongshe.com/reaction/2182506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoylhydrazineHCID 11955—
ReactantHCID 15408135HCID 15408135—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductHCID 10198473HCID 10198473—

Reaction Steps

2.5 g (11 mmol) of 5-(2-fluorobenzoyl)furan-2-carboxylic acid, 3.28 g (24 mmol) of benzhydrazide and 2 drops of glacial acetic acid in 50 ml of ethanol were heated under reflux for 10 h. The mixture was subsequently concentrated using a rotary evaporator and the residue was taken up in water, made alkaline using 2 N NaHCO3 solution and extracted with ethyl acetate. The aqueous phase was made acidic using 2 N hydrochloric acid and extracted with ethyl acetate. The combined organic phases were dried and concentrated using a rotary evaporator. The residue was dissolved in 25 ml of THF, 2.74 g (24.2 mmol) of potassium tert-butoxide were added and the mixture was stirred at reflux temperature for 1.5 h. After cooling, the mixture was concentrated using a rotary evaporator and the residue was taken up in 1 N aqueous sodium hydroxide solution and extracted with ethyl acetate. The precipitate that resulted when the aqueous phase was acidified was filtered off with suction, washed with water and dried in a vacuum drying cabinet at 40° C. This gave 1.88 g (75%) of the title compound. m.p.: 205° C. (decomp).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897232B2
Source datasetuspto-grants-2005_05
ORD IDord-d2ac91aead1a46299e456db0794b4980
Source noteuspto-grants-2005_05