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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255598Generated: October 31, 2026

Trimethylsilyl iodide → HCID 20183631, compound

https://huagongshe.com/reaction/255598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
Reactant3-ethoxycarbonyl-1-benzoyl-4H-quinolizin-4-oneHCID 15632074—
SolventChloroformHCID 6212—
ProductHCID 20183631HCID 2018363164.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-ethoxycarbonyl-1-benzoyl-4H-quinolizin-4-one (2.14 g) in chloroform (65 ml) was added dropwise trimethylsilyliodide (1.04 ml) at 0° C. After stirring for 30 minutes at 0° C., trimethylsilyliodide (1.04 ml) was added. After stirring for hour at room temperature, trimethylsilyliodide (1.04 ml) was added. After stirring for 2 hours at room temperature, the reaction mixture was diluted with chloroform and washed with water. After drying over magnesium sulfate, the chloroform extract was filtered and concentrated. The precipitate was washed with a cold chloroform to give 1-benzoyl-4H-quinolizin-4-one-3-carboxylic acid (1.252 g) as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04698349
Source datasetuspto-grants-1987_10
ORD IDord-79d8841f82eb4e608da942560e599f62
Source noteuspto-grants-1987_10