HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255598Generated: October 31, 2026
Trimethylsilyl iodide → HCID 20183631, compound
https://huagongshe.com/reaction/255598
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | 3-ethoxycarbonyl-1-benzoyl-4H-quinolizin-4-one | HCID 15632074 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 20183631 | HCID 20183631 | 64.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04698349 |
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| Source dataset | uspto-grants-1987_10 |
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| ORD ID | ord-79d8841f82eb4e608da942560e599f62 |
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| Source note | uspto-grants-1987_10 |
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