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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032254Generated: November 1, 2026

Water → HCID 11807407, compound

https://huagongshe.com/reaction/1032254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant1,4-CyclohexanedioneHCID 12511—
Reactant1-(2-Pyridyl)piperazineHCID 94459—
SolventAcetoneHCID 180—
SolventHydrochloric AcidHCID 313—
SolventTolueneHCID 1140—
ProductHCID 11807407HCID 11807407—

Reaction Steps

A solution of 1,4-cyclohexanedione monoethyleneketa (50.0 g), 1-(2-pyridyl)piperazine (52.16 g), and p-toluenesulfonic acid (0.5 g) in 500 ml of toluene is refluxed with a Dean-Stark trap until the theoretical amount of water is collected (about four hours). The solvent is evaporated in vacuo and the residue is dissolved in 750 ml of methanol. This solution is cooled in an ice bath and sodium cyanoborohydride (30.1 g) is added in small portions over a two-minute period. The resulting suspension is stirred mechanically and over the next 30 minutes enough concentrated hydrochloric acid solution is added dropwise to the reaction mixture to maintain a pH of about 4. The solvent is removed in vacuo to leave a semisolid residue which is dissolved in 300 ml of a 10% solution of hydrochloric acid in a well ventilated fume hood. This solution is diluted with an equal volume of acetone and refluxed for two hours. The volatile components of the mixture are removed in vacuo and the residue is cooled in an ice bath and made basic with concentrated ammonium hydroxide. The white solid which forms is recrystallized from ethyl acetate-heptane to give 52.4 g of the title compound; mp 142°-144° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04957921
Source datasetuspto-grants-1990_09
ORD IDord-72d21876a7744d4baba0815d308b0db1
Source noteuspto-grants-1990_09