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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214806Generated: November 2, 2026

Oxalyl chloride → 2-fur-2-yl-2-oxoacetic acid (3R)-1-azabicyclo[2.2.2]oct-3-yl ester

https://huagongshe.com/reaction/2214806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant2-Furylglyoxylic acidHCID 73846—
Reactant3-Quinuclidinol, (-)-HCID 91404—
CatalystDimethylformamideHCID 6228—
SolventChloroformHCID 6212—
Product2-fur-2-yl-2-oxoacetic acid (3R)-1-azabicyclo[2.2.2]oct-3-yl esterHCID 6659205352.8%

Reaction Steps

Oxalyl chloride (9.75 ml, 0.112 mol) was added to a solution of oxofuran-2-ylacetic acid (10 g, 0.071 mol) and dimethylformamide (one drop) in 150 ml of chloroform (etanol free) at 01 C. The mixture was stirred and allowed to warm at room temperature. After five hours the solvent was evaporated. The residue was dissolved in chloroform and evaporated again. This procedure was repeated two times. The product obtained was disolved in CHCl3 (150 ml) and a solution of 3(R)-quinuclidinol (10.90 g, 0.086 mol) in CHCl3 (150 ml) was added to this at 01 C. The mixture was stirred and allowed to warm at room temperature. After 15 h at r.t., the mixture was washed with 10% aqueous potassium carbonate, then with water, dried over Na2SO4 and evaporated to give 9.34 g (52.5%) of the title compound as a dark oil. Estructure confirmed by NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109210B2
Source datasetuspto-grants-2006_09
ORD IDord-5607c3ad70864ff0a95fdef06598dc3a
Source noteuspto-grants-2006_09