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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657623Generated: October 30, 2026

5-Aminovaleric acid → HCID 11978855, compound

https://huagongshe.com/reaction/657623

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Aminovaleric acidHCID 138—
ReactantSodium HydroxideHCID 14798—
ReactantOxalateHCID 71081—
ReactantHCID 2057368HCID 2057368—
SolventWaterHCID 962—
ProductHCID 11978855HCID 11978855—

Reaction Steps

A mixture of 1-(3-phenoxypropyl)piperidine, oxalate (0.2 g), 5-aminopentanoic acid (0.076 g) and polyphosphoric acid (2 g) is stirred at a temperature close to 100° C. for one hour. The mixture is cooled to room temperature, diluted with water (25 mL), made alkaline through addition of concentrated aqueous sodium hydroxide solution with external cooling and extracted twice with ethyl acetate (25 mL). The organic layers are pooled, washed with a saturated aqueous solution of sodium chloride (25 mL), dried over magnesium sulphate and purified by chromatography over silica gel. Fractions containing the expected product are pooled, concentrated under reduced pressure to give 0.172 g of 6-[4-(3-piperidinopropoxy)phenyl]-2,3,4,5-tetrahydropyridine which is dissolved in ethanol (2 mL). A solution of oxalic acid (0.104 g) in ethanol (0.5 mL) is added. The precipitate that appears on standing is filtered, rinsed with ethanol and dried to afford 200 mg of 6-[4-(3-piperidinopropoxy)phenyl]-2,3,4,5-tetrahydropyridine, oxalate as a white powder melting at 104° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076329B2
Source datasetuspto-grants-2011_12
ORD IDord-a47fc9583af543d6abd724edca09ab1a
Source noteuspto-grants-2011_12