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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49601Generated: October 25, 2026

Hydrochloric Acid → 3-Ethenyl-3-hydroxy-1-azabicyclo[2.2.2]octane

https://huagongshe.com/reaction/49601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant3-QuinuclidinoneHCID 19507—
ReactantHCID 178418507HCID 178418507—
SolventTetrahydrofuranHCID 8028—
Product3-Ethenyl-3-hydroxy-1-azabicyclo[2.2.2]octaneHCID 2262077854%

Reaction Steps

Under an argon atmosphere, a solution of 3-quinuclidinone (1.25 g, 10 mmol) in anhydrous tetrahydrofuran (10 mL) was added over 15 minutes to a 1 M solution of vinylmagnesium bromide in tetrahydrofuran (20 mL, 20 mmol) at 0° C. to 5° C., stirred at room temperature for 24 hours, cooled to 0° C., and acidified to pH 1 with 6 M hydrochloric acid. The mixture was stirred for 15 minutes, basified to pH 10 with 25% aqueous sodium hydroxide, extracted with chloroform (4×50 mL) and chloroform/methanol (4:1, 50 mL), combined the organic layers, dried (MgSO4), evaporated under reduced pressure and purified by flash chromatography (eluting with ammoniated chloroform/methanol, 85:15) to obtain the title compound (830 mg, 5.4 mmol, 54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706878B2
Source datasetuspto-grants-2004_03
ORD IDord-104634446aeb42d7ba0c56844f5c4ea7
Source noteuspto-grants-2004_03