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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52392Generated: October 25, 2026

Propargyl bromide → 2-Propargyloxy-2-phenyl-3-butyne

https://huagongshe.com/reaction/52392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantSodium HydroxideHCID 14798—
Reactant3-Hydroxy-3-phenyl-1-butyneHCID 92098—
ReactantTetrabutyl ammonium hydrogen sulfate waterHCID 86750630—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
Product2-Propargyloxy-2-phenyl-3-butyneHCID 1125239265%

Reaction Steps

Propargyl bromide (22 g, 0.15 mol) was dissolved in 140 ml of n-hexane. This solution, 2-phenyl-3-butyne-2-ol (14.6 g, 0.1 mol), NaOH (60 g, 1.5 mol) and a catalytic amount of tetrabutyl ammonium hydrogen sulfate/water (120 ml) were mixed, reacted for 24 hours at an ambient temperature and refluxed for 30 minutes. After completion of the reaction, the mixture was cooled to an ambient temperature and water (100 ml) was added. The organic phase was extracted with 30 ml of n-hexane, three times. The extracted organic solvent was dried with anhydrous magnesium sulfate, filtered and evaporated to separate. b.p.: 61° C./0.5 mmHg; yield: 65%; MS: m/e 184 (parent), 129 (base).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616669
Source datasetuspto-grants-1997_04
ORD IDord-0eda761b3ecf455a8a5934f3ae9aab88
Source noteuspto-grants-1997_04