HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657623Generated: October 30, 2026
5-Aminovaleric acid → HCID 11978855, compound
https://huagongshe.com/reaction/657623
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Aminovaleric acid | HCID 138 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Oxalate | HCID 71081 | — |
| Reactant | HCID 2057368 | HCID 2057368 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 11978855 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08076329B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-a47fc9583af543d6abd724edca09ab1a |
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| Source note | uspto-grants-2011_12 |
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