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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831970Generated: November 4, 2026

Methyl Acrylate → HCID 22050195, compound

https://huagongshe.com/reaction/1831970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcrylateHCID 7294—
ReactantTetramethoxysilaneHCID 12682—
ReactantCesium fluorideHCID 25953—
Reactant3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-oneHCID 22050429—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22050195HCID 2205019593.3%

Reaction Steps

3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (5.00 g, 17.85 mmol) and cesium fluoride (0.27 g, 1.78 mmol) were suspended in tetrahydrofuran (50 mL) followed by dropwise addition of tetramethylortho silicate (2.70 g, 17.85 mmol) at room temperature. After stirring for 10 minutes at room temperature, methyl acrylate (2.00 g, 23.20 mmol) was added dropwise and the reaction stirred at room temperature for 48 hours. 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 (6.10 g, 93%). 1H NMR (400 MHz, CDCl3) δ 7.42 (d, J=7.65 Hz, 1H), 7.41-7.29 (m, 5H), 6.04 (d, J=7.65 Hz, 1H), 5.20 (s, 2H), 4.17 (t, J=5.91 Hz, 2H), 3.63 (s, 3H), 2.85 (t, J=5.91 Hz, 2H). ES-HRMS m/z 366.0350 (M+H C16H16BrNO4 requires 366.0335).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067540B2
Source datasetuspto-grants-2006_06
ORD IDord-c05568444121457da07c25ab7664c7c1
Source noteuspto-grants-2006_06