Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205717Generated: November 2, 2026

(R)-Quinuclidin-3-yl ((S)-(3-(2-((4-(hydroxymethyl)phenyl)amino)-2-oxoethoxy)phenyl)(phenyl)methyl)carbamate → (R)-Quinuclidin-3-yl ((S)-(3-(2-((4-formylphenyl)amino)-2-oxoethoxy)phenyl)-(phenyl)methyl)carbamate

https://huagongshe.com/reaction/2205717

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-Quinuclidin-3-yl ((S)-(3-(2-((4-(hydroxymethyl)phenyl)amino)-2-oxoethoxy)phenyl)(phenyl)methyl)carbamateHCID 90204880—
CatalystHCID 178418406HCID 178418406—
Solvent1,4-DioxaneHCID 31275—
Product(R)-Quinuclidin-3-yl ((S)-(3-(2-((4-formylphenyl)amino)-2-oxoethoxy)phenyl)-(phenyl)methyl)carbamateHCID 90211965—

Reaction Steps

To a stirred solution of (R)-quinuclidin-3-yl ((S)-(3-(2-((4-(hydroxymethyl)-phenyl)amino)-2-oxoethoxy)phenyl)(phenyl)methyl)carbamate (0.68 g, 1.31 mmol) in 1,4-dioxane (10 mL) was added manganese (IV) oxide (0.57 g, 6.58 mmol). The reaction mixture was stirred at room temperature for 60 hours. The suspension was filtered and the filter cake was washed with ethyl acetate. The filtrate was evaporated at reduced pressure to afford the crude title compound. This material was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371318B2
Source datasetuspto-grants-2016_06
ORD IDord-9cca3271e79e4f3bad4d8854e40f27d6
Source noteuspto-grants-2016_06