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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1866962Generated: November 1, 2026

Tetraethoxysilane → HCID 22050002, compound

https://huagongshe.com/reaction/1866962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetraethoxysilaneHCID 6517—
ReactantEthyl AcrylateHCID 8821—
ReactantCesium fluorideHCID 25953—
Reactant3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-oneHCID 22050429—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22050002HCID 2205000292%

Reaction Steps

3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (0.50 g, 1.78 mmol) and cesium fluoride (0.0027 g, 0.178 mmol) were suspended in tetrahydrofuran (10 mL) followed by dropwise addition of tetraethylortho silicate (0.37 g, 1.78 mmol) at room temperature. After stirring for 10 minutes at room temperature, ethyl acrylate (0.23 g, 2.32 mmol) was added dropwise and the reaction stirred at room temperature overnight. The reaction mixture was filtered through a pad of Celite®. The filtrate was concentrated and the resulting residue subjected to chromatography (silica gel, ethyl acetate with 10% methanol/hexanes) to afford a white solid (0.62 g, 92%). 1H NMR (400 MHz, CDCl3) δ 7.42 (d, J=7.79 Hz, 1H), 7.41-7.29 (m, 5H), 6.03 (d, J=7.65 Hz, 1H), 5.20 (s, 2H), 4.17 (t, J=5.98 Hz, 2H), 4.07 (q, J=7.16 Hz, 2H), 2.83 (t, J=5.98 Hz, 2H), 1.19 (t, J=7.18 Hz, 3H) ES-HRMS In/z 380.0523 (M+H C17H18BrNO4 requires 380.0492).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629363B2
Source datasetuspto-grants-2009_12
ORD IDord-2993ad38256145d6a59284dacba44c3e
Source noteuspto-grants-2009_12