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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655329Generated: November 4, 2026

Hydrochloric Acid → HCID 13671866, compound

https://huagongshe.com/reaction/1655329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfurous AcidHCID 1100—
ReactantPiperidine-1-propylamineHCID 19049—
ReactantHCID 19791677HCID 19791677—
Reactant5-Methyl-1-phenylhexane-1,2-dioneHCID 19791681—
CatalystZincHCID 23994—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
ProductHCID 13671866HCID 1367186631%

Reaction Steps

To a refluxing mixture of 1-(3-aminopropyl)piperidine (284 mg, 2 mmol), sulfurous acid (6% SO2 aqueous solution) (1.1 ml) and zinc dust (200 mg) in methanol (2.5 ml) was added dropwise over a period of 1 hour a solution of 5-methyl-1-phenylhexane-1,2-dione [bp: 104°-107° C./2 mmHg; prepared from 2-bromo-5-methyl-1-phenylhexan-1-one by a known method {N. Kornblum and H. W. Frazier: J. Am. Chem. Soc., 88, 865 (1966)}] (275 mg, 1.35 mmol) in methanol (1.0 ml). Thereafter, 200 mg of zinc dust and 1.8 ml of sulfurous acid were freshly added to the mixture and the resulting mixture was refluxed for further 2 hours. After cooling, methanol was added to the mixture and insoluble material was removed by filtration. The filtrate was concentrated under reduced pressure and the residue was dissolved in 2N-HCl. The resulting solution was washed three times with ether and then basified with an aqueous sodium hydroxide solution, followed by extraction with ether. The combined ethereal extract was washed twice with water, dried over anhydrous sodium sulfate and evaporated under reduced pressure to give 0.43 g of oily matter. To an ethanol solution of the matter was added 6N-HCl in EtOH (0.64 ml) and the solution was allowed to stand. Precipitated crystals were collected by filtration and washed with ethanol to obtain 170 mg of the title compound as white crystals (yield: 31%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05250546
Source datasetuspto-grants-1993_10
ORD IDord-a9e63b33ffd74546a18c8ad74d18c7f2
Source noteuspto-grants-1993_10