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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Allylamino-1-(3-(s)-hydroxy-pyrrolidin-1-yl)-2-(s)-phenyl-ethanoneHCID 20756539—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20756538HCID 2075653868.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852713B2
Source datasetuspto-grants-2005_02
ORD IDord-610a9013493f4ad29eda5f303f2c0eda
Source noteuspto-grants-2005_02