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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900778Generated: October 30, 2026

Tetrahydrofuran → 3-(3,3-Diphenyl-1-butynyl)quinuclidin-3-ol

https://huagongshe.com/reaction/900778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHexaneHCID 8058—
Reactant1-azabicyclo[2.2.2]octan-2-oneHCID 566119—
Reactant(1-Methyl-1-phenyl-2-propynyl)benzeneHCID 10929756—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product3-(3,3-Diphenyl-1-butynyl)quinuclidin-3-olHCID 992426061%

Reaction Steps

(1-methyl-1-phenyl-2-propynyl)benzene (Dehmlow E., Tetrahedron Lett. (1971), 563-566) (380 mg, 1.84 mmol.) in THF (10 ml) at −78° C. was treated with a 1.6 N solution of BuLi in hexane (1.21 ml, 1.94 mmol). After 30 minutes, at the same temperature, a solution of quinuclidinone (300 mg, 2.4 mmol) in THF (5 ml) was added dropwise. After 1 hour, the reaction was left at room temperature for 12 hours. The mixture was then diluted with ether and washed with water (twice) and brine. The organic phase was dried over MgSO4 and evaporated to dryness. Chromatography on silica gel (elution: CH2Cl2/EtOH/NH4OH 90/10/0.1) gave 3-(3,3-diphenyl-1-butynyl)quinuclidin-3-ol 195 as a white solid (380 mg, 61%). This compound was used as such in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361668B2
Source datasetuspto-grants-2008_04
ORD IDord-62c944c1be1d4d4bb9cb042cbaa33ff7
Source noteuspto-grants-2008_04