HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485104Generated: November 1, 2026
Piperidine → 4-(Piperidine-1-carbonyl)benzaldehyde
https://huagongshe.com/reaction/1485104
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 4-Formylbenzoic acid | HCID 12088 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-(Piperidine-1-carbonyl)benzaldehyde | HCID 19069089 | 102.3% |
Reaction Steps
To a solution of 4-carboxybenzaldehyde (1.06 g) in chloroform (14.1 mL), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (2.03 g), 1-hydroxybenzotriazole monohydrate (1.62 g) and piperdine (1.05 mL) were added. After stirring the mixture at room temperature for 15 hours, a saturated aqueous solution of ammonium chloride was added. After extraction with ethyl acetate, the combined organic layers were washed with saturated brine. The washed organic layers were dried over anhydrous magnesium sulfate and after removing the desiccant by filtration, the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=85:15-30:70) to give the titled compound as a colorless oil (1.57 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422240B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-24f40f06325848508d6522151fc4e203 |
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| Source note | uspto-grants-2016_08 |
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