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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1967362Generated: October 31, 2026

Acetic Acid → 4-[(3S,4S,5S)-3-benzyl-4-hydroxy-5-methyl-2-oxopyrrolidin-1-yl]-2-chlorobenzonitrile

https://huagongshe.com/reaction/1967362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzyl BromideHCID 7498—
ReactantDiisopropylamineHCID 7912—
Reactant2-chloro-4-[(2S,3S)-3-hydroxy-2-methyl-5-oxopyrrolidin-1-yl]benzonitrileHCID 59556969—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-[(3S,4S,5S)-3-benzyl-4-hydroxy-5-methyl-2-oxopyrrolidin-1-yl]-2-chlorobenzonitrileHCID 5955699930%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of diisopropylamine (0.150 mL) in THF (8 mL) was cooled to −78° C., and n-butyllithium-hexane solution (0.648 mL, 1.6 mol/L) was added dropwise. After the completion of the dropwise addition, the mixture was stirred at −78° C. for 1 hr. Subsequently, a solution of 2-chloro-4-[(2S,3S)-3-hydroxy-2-methyl-5-oxopyrrolidin-1-yl]benzonitrile (100 mg) in THF (2.5 mL) was added dropwise, and the mixture was further stirred at −78° C. for 30 min. A solution of benzyl bromide (0.16 mL) in THF (1.5 mL) was added dropwise at −78° C., and the mixture was further stirred at −78° C. to −30° C. for 1 hr. Acetic acid (1.0 mL) was added to the reaction mixture, and the mixture was warmed to room temperature. Water was added, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=50/1→1/2) to give the title compound as a colorless solid (yield: 40.8 mg, 30.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420694B2
Source datasetuspto-grants-2013_04
ORD IDord-5358f2216c04454b8402b452f224e5a8
Source noteuspto-grants-2013_04