HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 233014Generated: October 26, 2026
5-(3-Methoxyphenyl)-2-pyrrolidinone → 2-(3-Methoxyphenyl)pyrrolidine
https://huagongshe.com/reaction/233014
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-(3-Methoxyphenyl)-2-pyrrolidinone | HCID 15293225 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(3-Methoxyphenyl)pyrrolidine | HCID 3613824 | — |
Reaction Steps
To a stirred solution of 5-(3-methoxyphenyl)-2-pyrrolidinone (5.00 g) and tetrahydrofuran (260 ml), at ambient temperature, under nitrogen, was added lithium aluminum hydride (39.3 ml, 1M in tetrahydrofuran). The mixture was heated under reflux for 6 hrs, cooled to ambient temperature, and aqueous tetrahydrofuran was added slowly. The suspension was concentrated, and the residue was dissolved in dilute aqueous sulfuric acid. The solution was made basic (pH 12) by the slow addition of aqueous sodium hydroxide solution. The mixture was extracted with dichloromethane (3 times) and ether (1 time). The combined organic extracts were washed with brine, dried over anhydrous potassium carbonate, filtered, and the filtrate was concentrated to give 2-(3-methoxyphenyl)pyrrolidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05591856 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-1f91cd3840a741008edee16b2802093a |
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| Source note | uspto-grants-1997_01 |
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