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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491516Generated: October 26, 2026

Hydrochloric Acid → 1-(4-Ethylphenyl)-4-(4-ethylcyclohexyl)-1-butyn-3-ol

https://huagongshe.com/reaction/1491516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Ethyl-4-ethynylbenzeneHCID 142425—
Reactant2-(4-Ethylcyclohexyl)acetaldehydeHCID 18952799—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Ethylphenyl)-4-(4-ethylcyclohexyl)-1-butyn-3-olHCID 1895282083.2%

Reaction Steps

4-Ethylphenylacetylene (1.3 g) was dissolved in THF (20 ml), followed by dropwise adding an n-butyllithium-hexane solution (1.61M, 0.62 ml) under ice cooling with stirring, further stirring the reaction solution under ice cooling for 30 minutes, dropwise adding a solution of 2-(4-ethylcyclohexyl)acetaldehyde (1.5 g) in THF (10 ml) , raising the temperature of the reaction solution up to room temperature after completion of the addition, stirring it for 5 hours, adding dilute hydrochloric acid (5 ml) to the resulting raw solution, extracting with ethyl acetate (50 ml), washing the organic layer with water, drying over anhydrous MgSO4 and concentrating under reduced pressure, to obtain a brown oil, which was then recrystallized from an ethyl acetate-heptane mixed solution, to obtain white crystals of 1-(4-ethylphenyl)-4-(4-ethylcyclohexyl)-1-butyn-3-ol (2.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05370819
Source datasetuspto-grants-1994_12
ORD IDord-71d355a32cda4a4aab7d7e37b752ce94
Source noteuspto-grants-1994_12