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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium CarbonateHCID 11430—
Reactant6-bromo-1-((2-(trimethylsilyl)ethoxy)methyl)quinolin-2(1H)-oneHCID 86679776—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Product1-((2-(trimethylsilyl)ethoxy)methyl)-6-vinylquinolin-2(1H)-oneHCID 8667977594%

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841301B2
Source datasetuspto-grants-2014_09
ORD IDord-8417f1ae5bab4f508b110ce8dfa9728e
Source noteuspto-grants-2014_09