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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837990Generated: October 26, 2026

Ammonium Chloride → (+/-)-(4R*,5R*)-5-((1S *)-Hydroxy-2-thienylmethyl)-1-methyl4-phenyl-pyrrolidin-2-one

https://huagongshe.com/reaction/1837990

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant(-)-(4R*,5R*)-5-formyl-1-methyl-4-phenylpyrrolidin-2-oneHCID 13825985—
ReactantLithium ThiopheneHCID 68750865—
SolventTetrahydrofuranHCID 8028—
Product(+/-)-(4R*,5R*)-5-((1S *)-Hydroxy-2-thienylmethyl)-1-methyl4-phenyl-pyrrolidin-2-oneHCID 1407142127%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a −50° C. solution of lithium thiophene (1M in THF, 170 mL, 170 mmol) was added a solution of (±)-(4R*,5R*)-5-formyl-1-methyl-4-phenylpyrrolidin-2-one (Intermediate Z, 127 mmol) in THF (10 mL). The reaction mixture was allowed to warm to 0° C. over 45 min and treated with a saturated NH4Cl solution. The resulting mixture was extracted with EtOAc, dried (MgSO4) and concentrated under reduced pressure. The crude product was purified by flash chromatography (67% EtOAc/hex) to give (±)-(4R*,5R*)-5-((1S*)-hydroxy-2-thienylmethyl)-1-methyl-4-phenylpyrrolidin-2-one (9.76 g, 27%): TLC (EtOAc) Rf 0.42.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06784167B2
Source datasetuspto-grants-2004_08
ORD IDord-a204989fae014c6f9382e8d6ac9655c6
Source noteuspto-grants-2004_08