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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037696Generated: October 31, 2026

Hydrochloric Acid → 3-(But-3-enyloxy)cyclooct-1-yne

https://huagongshe.com/reaction/1037696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant(E)-1-Bromo-8-(but-3-enyloxy)cyclooct-1-eneHCID 66672529—
SolventDimethyl SulfoxideHCID 679—
Product3-(But-3-enyloxy)cyclooct-1-yneHCID 8666425887.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

The compound 2 (2.04 g, 7.8 mmol) is dissolved in anhydrous DMSO (10 ml) and heated to 60° C. DBU (2.3 ml, 2 eq.) is added and the solution is stirred for 15 min. before adding further DBU (4.6 ml, 4 eq.) and again stirring for 15 min. Finally, DBU (4.6 ml, 4 eq.) is added a final time and the solution is stirred at 60° C. overnight and subsequently left to return to ambient temperature. 150 ml of AcOEt are added to this solution and extraction is carried out with HCl (1M). When the pH becomes basic, the organic phase is washed with water to neutrality. The extracted phase is dried over MgSO4, filtered and purified by flash chromatography (cyclohexane/AcOEt 99:1) in order to produce the compound 3 (1.22 g, 6.8 mmol, 87%), a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546598B2
Source datasetuspto-grants-2013_10
ORD IDord-8341a08d441a4daa800ca74bf3ae3d60
Source noteuspto-grants-2013_10