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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207685Generated: November 1, 2026

Propargyl bromide → 3-(Benzhydrylidene-amino)-1-methyl-3-prop-2-ynyl-pyrrolidin-2-one

https://huagongshe.com/reaction/2207685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant3-(Benzhydrylidene-amino)-1-methyl-pyrrolidin-2-oneHCID 89648998—
SolventIsopropanolHCID 3776—
SolventTetrahydrofuranHCID 8028—
Product3-(Benzhydrylidene-amino)-1-methyl-3-prop-2-ynyl-pyrrolidin-2-oneHCID 89649535—

Reaction Steps

Potassium tert-butoxide 1.7M in THF (32.8 mL, 55.76 mmol) was added dropwise over a period of 80 minutes (by syringe pump) to a solution of the 3-(benzhydrylidene-amino)-1-methyl-pyrrolidin-2-one (14.11 g, 50.692 mmol) (which may be prepared as described in Description 1) and propargyl bromide (6.78 mL, 60.83 mmol) in THF (250 mL) at 0° C. under nitrogen. The reaction was stirred for 2 hours. Additional KOtBu (5 ml) was added dropwise and stirring was continued for 15 mins. The reaction was quenched by the addition of satd. aq. NaHCO3 and diluted with EtOAc. The phases were separated, the organic layer was dried (Na2SO4) and the solvent evaporated to afford a crude brown oil which solidified on standing. This waxy-solid was suspended in IPA (approx. 30 ml) and stirred for 1 hr. The solid was filtered off, washed with a little IPA to afford 3-(benzhydrylidene-amino)-1-methyl-3-prop-2-ynyl-pyrrolidin-2-one (D2) as a light brown solid (6.26 g);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376445B2
Source datasetuspto-grants-2016_06
ORD IDord-6ebfd8c8a9084b0c83e611941aacfd55
Source noteuspto-grants-2016_06