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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12930Generated: October 29, 2026

Propargyl bromide → 3-[4-(4-Prop-2-ynyloxy-phenyl)-piperazin-1-yl]-propionic acid methyl ester

https://huagongshe.com/reaction/12930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantPotassium CarbonateHCID 11430—
Reactant3-[4-(4-Hydroxy-phenyl)-piperazin-1-yl]-butyric acid methyl esterHCID 68432675—
SolventDimethylformamideHCID 6228—
Product3-[4-(4-Prop-2-ynyloxy-phenyl)-piperazin-1-yl]-propionic acid methyl esterHCID 8661965739.7%

Reaction Steps

To a mixture of the compound from step 1 (278 mg, 1.0 mmol) and K2CO3 (152 mg, 1.1 mmol) in DMF (5 mL) was added 3-bromopropyne (130 mg, 1.1 mmol) dropwise at rt. The reaction mixture was stirred at rt overnight and then partitioned between water and ethyl acetate. The organic payers were combined and washed with brine, dried over anhydrous Na2SO4 and evaporated under vacuum to give a brown oil. The crude product was purified by silica gel flash chromatography (30% ethyl acetate in hexane) to furnish the title compound (120 mg, 38%) as a light yellow solid; MS; m/z 317 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728032B2
Source datasetuspto-grants-2010_06
ORD IDord-8ca57d439fb34165987b64e0ae661fb3
Source noteuspto-grants-2010_06