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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486482Generated: October 30, 2026

3-Quinuclidinol, (-)- → HCID 53767445, compound

https://huagongshe.com/reaction/486482

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Quinuclidinol, (-)-HCID 91404—
Reactantphenylacetic anhydrideHCID 316205—
SolventEthyl AcetateHCID 8857—
ProductHCID 53767445HCID 5376744593.3%

Reaction Steps

Phenylacetic acid anhydride (prepared as described in J. Org. Chem., 1588, 30, 1965) (15 g) was added to a suspension of (R)-3-quinuclidinol (5 g) in ethyl acetate (250 ml) at room temperature. After 178 hour the solvent was evaporated and the residue dissolved in hydrochloric acid (2M). This was washed with ethyl acetate, basified with sodium carbonate and extracted with ethyl acetate. The organic extract was dried over sodium sulphate and evaporated to give the title compound as a yellow oil (9 g, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292749
Source datasetuspto-grants-1994_03
ORD IDord-f4cdc91e3d5149b9b2bd69366e8a6f3d
Source noteuspto-grants-1994_03