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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409649Generated: October 29, 2026

3-Quinuclidinone → 3-Quinuclidinol, (-)-

https://huagongshe.com/reaction/409649

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-QuinuclidinoneHCID 19507—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178418361HCID 178418361—
SolventIsopropanolHCID 3776—
Product3-Quinuclidinol, (-)-HCID 91404—

Reaction Steps

1.63 g (13 mmol) of the 3-quinuclidinone (I), 1.1 mg (1.3 μmol) of {[(S)-(6,6′-dimethyl-1,1′-biphenyl-2,2′-diyl)-bis(diphenylphosphine)]ruthenium (II) dichloride (DMF)n} complex, 12.7 ml of 2-propanol and 31 μl (1.55 μmol) of a 0.05 M 2-propanol solution of (2R,3R,4R,5R)-3,4-O-isopropylidenehexane-2,5-diamine were added to an autoclave in which the inside had been replaced with argon followed by carrying out a degassing procedure and stirring for 30 minutes at room temperature. 0.26 mL (0.26 mmol) of a 2-propanol solution of potassium tert-butoxide (1.0 M) were added thereto followed by stirring for 16 hours at 20 to 25° C. at a hydrogen pressure of 2.0 MPa to obtain (R)-3-quinuclidinol (3-R). S/C, conversion rate and enantiomeric excess are indicated below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759524B2
Source datasetuspto-grants-2014_06
ORD IDord-ba19e5fe18bc4cc0a9db2aa7baddadc1
Source noteuspto-grants-2014_06