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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596678Generated: November 1, 2026

4-Cyanobenzoyl chloride → 9-(4-Cyanobenzoyl)-3-oxo-1-oxa-4,9-diaza-spiro[5.5]undecane

https://huagongshe.com/reaction/1596678

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Cyanobenzoyl chlorideHCID 80172—
ReactantHCID 23435708HCID 23435708—
SolventPyridineHCID 1049—
Product9-(4-Cyanobenzoyl)-3-oxo-1-oxa-4,9-diaza-spiro[5.5]undecaneHCID 23435702—

Reaction Steps

18.0 g (71.7 mmol) 3-oxo-1-oxa-4,9-diaza-spiro[5.5]undecane hydrobromide (prepared according to J. Med. Chem. 1983, 26, 855) were dissolved in 300 ml dry pyridine, and 11.9 g (71.9 mmol) 4-cyanobenzoyl chloride were added in small portions. The mixture was stirred over night at room temperature and evaporated under reduced pressure. The residue was dissolved in toluene, which was removed in vacuo. This process was repeated two times to remove remaining pyridine. It was treated with water and neutralized by addition of saturated aqueous sodium bicarbonate solution. The precipitate of the title compound was filtered with suction, washed with water, and dried in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291469B1
Source datasetuspto-grants-2001_09
ORD IDord-608d15803eef4ff49fc7987e15d3c8fe
Source noteuspto-grants-2001_09