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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655328Generated: November 1, 2026

Hydrochloric Acid → HCID 13671866, compound

https://huagongshe.com/reaction/1655328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPiperidine-1-propylamineHCID 19049—
ReactantHCID 19791712HCID 19791712—
SolventEthanolHCID 702—
ProductHCID 13671866HCID 1367186635%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 2-bromo-5-methyl-1-phenylhexan-1-ol [prepared from 2-bromo-5-methyl-1-phenylhexan-1-one by usual NaBH4 -reduction] (1.0 g, 3.69 mmol) and 1-(3-aminopropyl)piperidine (1.05 g, 7.38 mmol) was heated at 110° C. for 4 hours in a nitrogen atmosphere. After being cooled, the reaction mixture was dissolved in lN-HCl (50 ml) and the solution was washed with ether. The aqueous layer was basified with lN-NaOH and then extracted twice with ether. The combined ethereal extract was washed three times with water, dried over anhydrous sodium sulfate and evaporated under reduced pressure. The residue was purified by preparative TLC to give pale yellow oily matter. To a solution of the matter in ethanol was added in excess 18% HCl in EtOH and the resulting mixture was evaporated under reduced pressure. The residue was dissolved with heating in ethanol (15 ml) and to the mixture was then added 10 ml of acetone. The mixture was stirred at room temperature. Precipitated crystals were collected by filtration to obtain 0.52 g of the title compound (yield: 35%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05250546
Source datasetuspto-grants-1993_10
ORD IDord-7f85dc92a3c942ee86330729871835d4
Source noteuspto-grants-1993_10