Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491517Generated: November 1, 2026

Hydrochloric Acid → 1-(4-Trimethylsilyloxycyclohexyl)-4-(4-pentylcyclohexyl)-1-butyn-3-ol

https://huagongshe.com/reaction/1491517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-PentylcyclohexaneacetaldehydeHCID 13999085—
Reactant4-TrimethylsilyloxycyclohexylacetyleneHCID 18952792—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Trimethylsilyloxycyclohexyl)-4-(4-pentylcyclohexyl)-1-butyn-3-olHCID 1895286663.7%

Reaction Steps

4-Trimethylsilyloxycyclohexylacetylene (20 mmol) was dissolved in THF (20 ml), followed by dropwise adding a n-butyllithium-hexane solution (1.61M, 12.4 ml) while stirring the above solution under ice cooling, stirring the reaction solution under ice cooling for 30 minutes, dropwise adding a solution of 2-(4-pentylcyclohexyl)acetaldehyde (4.0 g) in THF (10 ml), raising the temperature of the reaction solution up to room temperature after completion of the dropwise addition, stirring it for 5 hours, adding dilute hydrochloric acid (5 ml) to the resulting raw solution, extracting the mixture with ethyl acetate (150 ml), washing the organic phase with water, drying over anhydrous MgSO4, concentrating under reduced pressure to obtain a brown oil, which is recrystallized from a mixed solution of ethyl acetate-heptane, to obtain 1-(4-trimethylsilyloxycyclohexyl)-4-(4-pentylcyclohexyl)-1-butyn-3-ol (5.0 g) (white crystal).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05370819
Source datasetuspto-grants-1994_12
ORD IDord-4eca8499336243f7a907755a7d8bd002
Source noteuspto-grants-1994_12