Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294976Generated: October 30, 2026

Methanol → 3-Ethynyl-1-azabicyclo[2.2.2]octan-3-ol

https://huagongshe.com/reaction/2294976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant3-QuinuclidinoneHCID 19507—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantButyllithiumHCID 178418339—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
Product3-Ethynyl-1-azabicyclo[2.2.2]octan-3-olHCID 3613517—

Reaction Conditions

Temperature-70 °C

Reaction Steps

A solution of n-butyl lithium (100 ml of a 2M solution in pentane) was added portion-wise over a period of 20 minutes to a stirred solution of ethynyltrimethylsilane (19.6 g) in dry tetrahydrofuran (400 ml) at -70° C. The mixture was stirred for 1 hour at -70° C. A solution of 3-quinuclidinone (2.4 g) in dry tetrahydrofuran (100 ml) was then added and the mixture stirred for 1 hour at -70° C. Methanol (1 ml) was then added to the mixture and the mixture allowed to warm to ambient temperature. The solvents were removed by evaporation. Methanol (500 ml) and potassium carbonate (40 g) were added to the residue and the mixture was stirred for 1 hour. The solvent was removed by evaporation. The residue was triturated with water (500 ml) and then dried in vacuo to give 3-ethynyl-3-hydroxy-quinuclidine as a solid, m.p. 193°-197° C.; NMR(DMSO-d6): 1.5-1.3(1H,m), 1.4-1.6(1H,m), 1.7-1.95(3H,m), 2.55-2.8(5H,m), 2.95(1H,d), 3.3(1H,d) and 5.4(1H,s); m/z 152 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05691349
Source datasetuspto-grants-1997_11
ORD IDord-4a8ac152af324d63a4c48ce06a4cb4fa
Source noteuspto-grants-1997_11