Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77053Generated: October 26, 2026

Triphenylphosphine → (R)-((R)-quinuclidin-3-yl) 2-(4-fluorophenylamino)-2-phenylacetate

https://huagongshe.com/reaction/77053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant3-Quinuclidinol, (+)-HCID 736411—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant(R)-(4-fluoro-phenylamino)-phenyl-acetic acidHCID 7006576—
SolventTetrahydrofuranHCID 8028—
Product(R)-((R)-quinuclidin-3-yl) 2-(4-fluorophenylamino)-2-phenylacetateHCID 5940113379.2%

Reaction Steps

To a solution of (R)-(4-fluoro-phenylamino)-phenyl-acetic acid (I253) (420 mg, 1.71 mmol) in dry THF (40 mL), are sequentially added (S)-quinuclidin-3-ol (218 mg, 1.71 mmol), DEAD (407 ul, 2.57 mmol) and triphenylphosphine (674 mg, 2.57 mmol). The reaction is refluxed for 30 minutes under N2 flowstream and then the solvent is evaporated. The residue is partitioned between water and EtOAc, the organic layer is separated, dried over Na2SO4, filtered and evaporated to dryness. The resulting crude is purified by flash chromatography (DCM/MeOH=95/5) to obtain the title compound as a pale yellow oil (480 mg, 79% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835682B2
Source datasetuspto-grants-2014_09
ORD IDord-dc805f9e25c4444591a87322ff5bb48d
Source noteuspto-grants-2014_09