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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576328Generated: November 3, 2026

Water → 1-(2-Furoyl)piperazine

https://huagongshe.com/reaction/1576328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPiperazineHCID 4837—
ReactantSodium HydroxideHCID 14798—
Reactant2-Furancarbonyl chlorideHCID 68242—
SolventAcetoneHCID 180—
Product1-(2-Furoyl)piperazineHCID 550206—

Reaction Steps

To a solution of 21.5 g. (0.25 mol) of piperazine in a mixture of 960 ml. of acidified water (pH = 4.5) and 1200 ml. of acetone, 32.5 g. (0.25 mol) of furoyl chloride are added dropwise while the pH is maintained at 4.5 by dropwise addition of a sodium hydroxide solution. The mixture is made alkaline, and extracted several times with chloroform. The chloroform is distilled off and the concentrated extract is distilled in vacuo. 18.3 g. of the N-(2-furoyl)piperazine thus obtained in 50 ml. of diethyl ether are added to an equivalent amount of cyanogen bromide in a mixture of 60 ml. of water and 60 ml. of diethyl ether. The mixture is stirred overnight at room temperature and then subjected to continuous extraction with benzene. The extract is dried over sodium sulphate and the solvent is distilled off. According to the NMR and IR spectra the residue consists of 1-cyano-4-(2-furoyl)piperazine, m.p. 63°-65°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03980650
Source datasetuspto-grants-1976_09
ORD IDord-0418f104636748d8bfcdbeaa165d81c1
Source noteuspto-grants-1976_09