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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77007Generated: October 26, 2026

Acetic Acid → (R)-Quinuclidin-3-yl 2-(4-methylbenzylamino)-2-phenylacetate

https://huagongshe.com/reaction/77007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-MethylbenzaldehydeHCID 7725—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(R)-quinuclidin-3-yl 2-amino-2-phenylacetateHCID 59401091—
SolventTetrahydrofuranHCID 8028—
SolventCyclohexaneHCID 8078—
Product(R)-Quinuclidin-3-yl 2-(4-methylbenzylamino)-2-phenylacetateHCID 5940111554.9%

Reaction Steps

To a solution of amino-phenyl-acetic acid (R)-(1-aza-bicyclo[2.2.2]oct-3-yl)ester (I76) (100 mg, 0.38 mmol) in dry THF (3.84 mL), are added 4-methylbenzaldehyde (68 mL, 0.57 mmol) and AcOH (0.5 mL, 8.73 mmol). The mixture is stirred at RT and sodium triacetoxyborohydride (163 mg, 0.77 mmol) is added. The reaction is stirred at RT for 1.5 hours then cyclohexane is added and the mixture is evaporated to dryness. The crude is purified by flash chromatography (DCM/MeOH/NH4OH=95/5/0.5) to obtain the title compound as a colorless oil (76 mg, 54% yield, mixture of diastereoisomers).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835682B2
Source datasetuspto-grants-2014_09
ORD IDord-74b3e9a6b35b420ca4eddb16d9a94bcb
Source noteuspto-grants-2014_09