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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | 1-[4-(4-Chloro-phenoxy)-phenyl]-pyrrolidine-2,5-dione | HCID 21834838 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[4-(4-Chloro-phenoxy)-phenyl]-5-hydroxy-pyrrolidin-2-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431607B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-2e20e13a73174ad3966116933f724496 |
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| Source note | uspto-grants-2013_04 |
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