HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77484Generated: October 28, 2026
Toluene → 1-((2-(trimethylsilyl)ethoxy)methyl)-6-vinylquinolin-2(1H)-one
https://huagongshe.com/reaction/77484
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-bromo-1-((2-(trimethylsilyl)ethoxy)methyl)quinolin-2(1H)-one | HCID 86679776 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-((2-(trimethylsilyl)ethoxy)methyl)-6-vinylquinolin-2(1H)-one | HCID 86679775 | 94% |
Reaction Steps
To a solution of 6-bromo-1-((2-(trimethylsilyl)ethoxy)methyl)quinolin-2(1H)-one (1 g, 2.82 mmol) in toluene (20 mL) and water (20.00 mL) were added trivinylboraxin (0.684 g, 4.23 mmol), K2CO3 (0.780 g, 5.64 mmol). The reaction mixture was purged with N2 for 15 min, then Tetrakis (0.652 g, 0.564 mmol) was added and the reaction mixture was heated to 110° C. for 12 h. The reaction mixture was concentrated and dissolved in ethyl acetate and washed with water. The organic layer was dried over anhydrous sodium sulfate, and concentrated to get the 1-((2-(trimethylsilyl)ethoxy)methyl)-6-vinylquinolin-2(1H)-one (0.8 g, 94%), used without further purification. LCMS (ES-API), RT: 2.17 m/z 302.2 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841301B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-8417f1ae5bab4f508b110ce8dfa9728e |
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| Source note | uspto-grants-2014_09 |
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