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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901504Generated: October 30, 2026

Sodium Carbonate → 1-(Tetrahydro-2-furoyl)piperazine

https://huagongshe.com/reaction/1901504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantSodium HydroxideHCID 14798—
Reactant1-(2-Furoyl)piperazineHCID 550206—
Reactant1-(2-Tetrahydrofuroyl)piperazine hydrobromideHCID 16217252—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product1-(Tetrahydro-2-furoyl)piperazineHCID 2734641—

Reaction Steps

The furoylpiperazine of Example 1 was converted to the hydrobromide salt (m.p. 173°-175° C.). This salt (39.0 g) in 250 ml methyl alcohol and 9.0 g Raney nickel was hydrogenated at 3 atm. After uptake of H2 ceased, the catalyst was filtered, the solvent concentrated, and the residue crystallized from isopropyl alcohol to give 35.2 g. tetrahydrofuroylpiperazine HBr, m.p. 152°-156° C. This was suspended in 20 ml H2O. Then 10.5 g 50%, NaOH solution was added slowly followed by 2.0 g solid Na2CO3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05578611
Source datasetuspto-grants-1996_11
ORD IDord-79cc97f8fd234e2b8dae7b0e0f09abee
Source noteuspto-grants-1996_11