HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23587Generated: October 28, 2026
2-Allylamino-1-(3-(s)-hydroxy-pyrrolidin-1-yl)-2-(s)-phenyl-ethanone → HCID 20756538, compound
https://huagongshe.com/reaction/23587
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Allylamino-1-(3-(s)-hydroxy-pyrrolidin-1-yl)-2-(s)-phenyl-ethanone | HCID 20756539 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20756538 | HCID 20756538 | 68.3% |
Reaction Steps
To a stirred solution of 2-allylamino-1-(3-(S)-hydroxy-pyrrolidin-1-yl)-2-(S)-phenyl-ethanone (5.65 g, 15.1 mmol) in anhydrous tetrahydrofuran (60 cm3) cooled to 0° C. in an ice bath was added a 1 M solution of lithium aluminum hydride (22.6 cm3, 22.7 mmol) over 20 minutes. The solution was allowed to warm and stir at ambient temperature for 16 hours. The reaction was cooled to 0° C. in an ice bath and quenched with water (0.860 cm3), 15% sodium hydroxide (0.860 cm3) and water (2.60 cm3) to form a white flocculate precipitate. The mixture was vacuum filtered, the precipitate washed with tetrahydrofuran (5×30 cm3) and the filtrate volatile fractions removed in vacuo to afford a crude yellow oil. The crude product was purified by column chromatography (silica, eluting with dichloromethane-methanol-ammonium hydroxide 97:3:0 to 90:10:1) to afford the title compound as a yellow viscous oil (2.54 g, 68.3%) with a positive ion ESI (M+H)+247.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06852713B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-610a9013493f4ad29eda5f303f2c0eda |
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| Source note | uspto-grants-2005_02 |
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