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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972187Generated: October 30, 2026

Nitrogen → 1-[4-(4-Chloro-phenoxy)-phenyl]-5-hydroxy-pyrrolidin-2-one

https://huagongshe.com/reaction/1972187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantDiisobutylaluminum hydrideHCID 14487—
Reactant1-[4-(4-Chloro-phenoxy)-phenyl]-pyrrolidine-2,5-dioneHCID 21834838—
SolventDichloromethaneHCID 6344—
Product1-[4-(4-Chloro-phenoxy)-phenyl]-5-hydroxy-pyrrolidin-2-oneHCID 59485616—

Reaction Steps

A solution of 1-[4-(4-chloro-phenoxy)-phenyl]-pyrrolidine-2,5-dione (100 mg, 0.33 mmol) in anhydrous CH2Cl2 (1.5 mL) is cooled down to −78° C. in a dry ice bath. DIBAL-H (0.6 mL, 1 M solution in hexane, 0.66 mmol) is added into the solution dropwise under N2. After the addition, the mixture is stirred at the same temperature for 10 min and quenched by H2O (10 mL). The mixture is warmed up to room temperature and extracted with CH2Cl2 (3×10 mL). The combined organic layer is washed with brine and dried (MgSO4). After filtering the drying agent, the filtrate is concentrated and purified by flash column chromatography (silica gel, EtOAc) to provide the (±)-1-[4-(4-chloro-phenoxy)-phenyl]-5-hydroxy-pyrrolidin-2-one as off white solid (72 mg, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431607B2
Source datasetuspto-grants-2013_04
ORD IDord-2e20e13a73174ad3966116933f724496
Source noteuspto-grants-2013_04