HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54469Generated: October 25, 2026
Ammonium formate → 2-(Pyrrolidin-3-yl)pyridine
https://huagongshe.com/reaction/54469
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 2-(1-Benzylpyrrolidin-3-yl)pyridine | HCID 10955622 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(Pyrrolidin-3-yl)pyridine | HCID 5013938 | 75% |
Reaction Steps
To a suspension of 2-[1-(phenylmethyl)-3-pyrrolidinyl]pyridine (7.15 g, 30.0 mmol) and 10% palladium on charcoal catalyst (1.90 g) in methanol (120 mL) was added dropwise a solution of ammonium formate (7.57 g, 120 mmol) in water (30 mL). The mixture was heated at reflux for 30 minutes, allowed to cool to room temperature, and filtered. The filtrate was concentrated under reduced pressure, the residue was taken up in water (10 mL), and the solution was made basic with concentrated ammonia and extracted with dichloromethane (4×15 mL). The organic extracts were combined, dried over anhydrous potassium carbonate, and concentrated to a yellow oil. This crude product was chromatographed (silica gel, chloroform-methanol-ammonia 75:25:5) to give the title compound (3.33 g, 75%) as a faint yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05622966 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-d9df612e9c6a45d9938703ca0ca2de1f |
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| Source note | uspto-grants-1997_04 |
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