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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242010Generated: October 30, 2026

1,4-Dioxa-8-azaspiro(4.5)decane → 1-(5-Fluoroquinolin-8-yl)piperidin-4-one

https://huagongshe.com/reaction/2242010

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxa-8-azaspiro(4.5)decaneHCID 67435—
Reactant8-Bromo-5-fluoroquinolineHCID 14548347—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTetrahydrofuranHCID 8028—
Product1-(5-Fluoroquinolin-8-yl)piperidin-4-oneHCID 59204848—

Reaction Conditions

Temperature66 °C

Reaction Steps

To a 2-L reactor with a stirrer, a thermocouple, a condenser and nitrogen inlet were charged 8-bromo-5fluoroquinoline (50 g), tetrahydrofuran (795 g), Pd2(dba)3 (3.78 g), Cymap (1.6 g), and 1,4-Dioxa-8-azaspiro[4.5]decane (47.3 g). the mixture was heated to reflux (66° C.) and the reaction was complete. The reaction mixture was quenched into a 5 L reactor containing 1000 g of water and 640 g of MTBE. The bottom aqueous layer was split off and the organic layer was washed with 5% NaOH (1120 g) and 20% NaCl (2×100 g). The solvent was evaporated, weight 87 g vs 79.4 g by theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07671056B2
Source datasetuspto-grants-2010_03
ORD IDord-0d460ed6d61c44a69675e58821272a43
Source noteuspto-grants-2010_03