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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341142Generated: November 1, 2026

Hydrazine hydrate (1:1) → (5S)-5-(aminomethyl)-3-(3-fluorophenyl)-1,3-oxazolidin-2-one

https://huagongshe.com/reaction/341142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant(5R)-2-[3-(3-fluoro-phenyl)-2-oxo-oxazolidin-5-ylmethyl]-isoindole-1,3-dioneHCID 68535606—
SolventEthanolHCID 702—
Product(5S)-5-(aminomethyl)-3-(3-fluorophenyl)-1,3-oxazolidin-2-oneHCID 1140155996.6%

Reaction Steps

A solution of phthalimide 110 (3.0 g, 8.82 mmol) in ethanol (EtOH, 30 mL) was treated with hydrazine monohydrate (2.20 g, 2.2 mL, 44.12 mmol, 5.0 equiv) at 25° C., and the resulting reaction mixture was warmed to reflux for 2 h. White precipitates formed as the reaction mixture was refluxed. When TLC and HPLC showed the reaction was complete, the reaction mixture was cooled to room temperature before being quenched with H2O (20 mL). The aqueous solution was then extracted with CH2Cl2 (3×40 mL), and the combined organic extracts were washed with H2O (2×20 mL) and saturated aqueous NaCl (20 mL), dried over MgSO4, and concentrated in vacuo. The residue was further dried in vacuo to afford the desired (5S)-5-aminomethyl-3-(3-fluoro-phenyl)-oxazolidin-2-one 111 (1.79 g, 96.6% yield) as a white powder. This product was directly used in the subsequent reactions without further purification. C10H11FN2O2, LCMS (EI) m/e 211 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895741B2
Source datasetuspto-grants-2014_11
ORD IDord-850cd2745edc42768da51cbf0e641a50
Source noteuspto-grants-2014_11