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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273194Generated: October 30, 2026

Triphenylphosphine → 4-Butyl-1-phenylpyrrolidin-2-one

https://huagongshe.com/reaction/273194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant3-Hydroxymethylheptanoic acid phenylamideHCID 69312033—
SolventTetrahydrofuranHCID 8028—
Product4-Butyl-1-phenylpyrrolidin-2-oneHCID 1795243872%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-hydroxymethylheptanoic acid phenylamide (0.61 g, 2.6 mmol) in THF (30 mL) under argon was added triphenylphosphine (1.36 g, 5.2 mmol). The solution was cooled to 0° C. and diethyl azodicarboxylate (0.61 mL, 3.9 mmol) was added dropwise. The reaction mixture was warmed up to rt and stirred overnight. The reaction was quenched with saturated aqueous NaHCO3 (50 mL) and extracted with dichloromethane (3×50 mL). The combined extractions were dried (Na2SO4), filtered and concentrated. The residue was purified by flash column chromatography (silica gel, ethyl acetate/hexanes 1:2) to afford 4-butyl-1-phenylpyrrolidin-2-one as a white solid (0.4 g, 72%). MS(ES) m/e 218 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456211B2
Source datasetuspto-grants-2008_11
ORD IDord-8d43c8feb4254c3b9264d070f66bb0fa
Source noteuspto-grants-2008_11