HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420597Generated: November 2, 2026
Water → 2-(1-Benzyl-4-pyrrolidine-1-ylpiperidine-4-yl)ethanol
https://huagongshe.com/reaction/420597
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 66658050 | HCID 66658050 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(1-Benzyl-4-pyrrolidine-1-ylpiperidine-4-yl)ethanol | HCID 66658038 | — |
Reaction Steps
Lithium aluminium hydride (324 mg) was suspended in tetrahydrofuran (25 mL). A solution of (1-benzyl-4-pyrrolidine-1-ylpiperidine-4-yl)acetic acid methyl ester (2.70 g) in tetrahydrofuran (25 mL) was added thereto at 0° C. After stirring at 0° C. for 1 hour, to the reaction solution were sequentially added with water (0.35 mL), 10% aqueous sodium hydroxide (0.35 mL) and water (1.05 mL). The insoluble material was filtrated and the filtrate was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over sodium sulphate. The solvent was evaporated under reduced pressure to give the title compound. The obtained objective substance was provided to the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08097610B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-dc0b0ac85b6b4d869036be129fc3bf47 |
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| Source note | uspto-grants-2012_01 |
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