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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166626Generated: November 4, 2026

Propargyl bromide → HCID 15571563, compound

https://huagongshe.com/reaction/2166626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantPotassium CarbonateHCID 11430—
Reactant3-[4-(1,1-Dimethylheptyl)-2-hydroxyphenyl]-1,2,5,6-tetrahydropyridineHCID 15571561—
SolventEthanolHCID 702—
ProductHCID 15571563HCID 15571563—

Reaction Steps

A mixture of 1.0 g. (3.33 mmoles) of 3-[4-(1,1-dimethylheptyl)-2-hydroxyphenyl]-1,2,5,6-tetrahydropyridine, 539 mg. (3.90 mmoles) of anhydrous potassium carbonate and 395 mg. (3.32 mmoles) of 1-bromo-2-propyne in 23 ml. of ethanol is heated at reflux for 20 hours. The reaction mixture is evaporated and dissolved in 100 ml. of saturated sodium bicarbonate and 200 ml. of dichloromethane. The organic extract is washed with two 150 ml. portions of saturated sodium chloride, dried over magnesium sulfate and evaporated. The residue is crystallized from pentane to yield 161 mg. of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04387229
Source datasetuspto-grants-1983_06
ORD IDord-5be9fe8207cd411f8d4aab833ef091eb
Source noteuspto-grants-1983_06