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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900774Generated: October 25, 2026

Hexane → 1-cycloheptyl-3-[(3R)-3-methoxy-1-azabicyclo[2.2.2]oct-3-yl]-1-phenyl-2-propyn-1-ol

https://huagongshe.com/reaction/900774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantCycloheptyl(phenyl)methanoneHCID 297753—
Reactant(3R)-3-ethynyl-1-azabicyclo[2.2.2]oct-3-yl methyl etherHCID 9812856—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-cycloheptyl-3-[(3R)-3-methoxy-1-azabicyclo[2.2.2]oct-3-yl]-1-phenyl-2-propyn-1-olHCID 69292392—

Reaction Conditions

Temperature-5 °C

Reaction Steps

A 1.6 N solution of BuLi in hexane (41.7 ml, 66.7 mmol) was added dropwise to a solution of (3R)-3-ethynyl-1-azabicyclo[2.2.2]oct-3-yl methyl ether 53 (11 g, 66.7 mmol) in THF (100 ml) cooled at −5° C. After stirring for 10 minutes, the medium was cooled at −15° C., and a solution of cycloheptyl(phenyl)methanone 44 (14.2 g, 70.2 mmol) in THF (50 ml) was slowly added. The cooling bath was removed and the reaction was allowed to gradually warm to room temperature during 2 hours. The reaction was quenched by the addition of saturated aqueous NH4Cl solution. The reaction mixture was washed with brine, dried over Na2SO4 and evaporated. The yellowish oil was purified by chromatography over silica gel (CH2Cl2/EtOH/NH4OH 94/6/1). 1-cycloheptyl-3-[(3R)-3-methoxy-1-azabicyclo[2.2.2]oct-3-yl]-1-phenyl-2-propyn-1-ol 116 was obtained as a white solid (20.35 g, 83%, mixture of diastereomers).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361668B2
Source datasetuspto-grants-2008_04
ORD IDord-0b5f7c8ca8064a15b6e47d696e40695f
Source noteuspto-grants-2008_04