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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296013Generated: October 31, 2026

Propargyl bromide → 1-(Prop-2-yn-1-yl)piperidin-2-one

https://huagongshe.com/reaction/2296013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
Reactant2-PiperidoneHCID 12665—
ReactantSodium hydrideHCID 24758—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
Product1-(Prop-2-yn-1-yl)piperidin-2-oneHCID 13289794—

Reaction Conditions

Temperature15 °C

Reaction Steps

Sodium hydride (5.76 g of 50% dispersion in oil, 0.12 mole) was washed three times with hexane and suspended in 645 ml of toluene. 2-Piperidone (11.88 g, 0.12 mole) in 100 ml of toluene was added to the well stirred sodium hydride suspension and heated to reflux for 2 hours. The reaction mixture was cooled to 15° C. and 2-propynyl bromide (14.28 g, 0.12 mole) in 55 ml of toluene added over 30 minutes. The mixture was then stirred at room temperature for 19 hours, filtered and mother liquor evaporated to yield a first batch of 1-(2-propynyl)-2-piperidone as an oil (7.87 g of about 55% purity by pnmr assay).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04427679
Source datasetuspto-grants-1984_01
ORD IDord-d4d90c506337401c81f2eb2abdb85b3d
Source noteuspto-grants-1984_01