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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831955Generated: October 31, 2026

Sodium hydride → HCID 11352784, compound

https://huagongshe.com/reaction/1831955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantBenzene, 1,3-bis(bromomethyl)-HCID 69373—
Reactant3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-oneHCID 22050429—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 11352784HCID 1135278438.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (2 g, 6.06 mmol) was suspended in 1,4-dioxane (250 mL). α,α′-Dibromo-m-xylene (8 g, 30.3 mmol) was added followed by sodium hydride (0.3 g, 7.5 mmol, 60% in mineral oil). The reaction was heated to 60° C. and stirred for 16 hours. The reaction was filtered through Celite® and the filtrate was concentrated to an oil that was partitioned between water and dichloromethane and extracted with dichloromethane (4×250 mL). The organic extracts were combined, washed with brine, dried over Na2SO4, and filtered. The filtrate was concentrated to an oil, and purified by chromatography (silica gel, hexane/ethyl acetate) to yield a white solid (1.2 g, 38%). 1H NMR (400 MHz, CDCl3) δ 7.57 (app q, J=7.6 Hz, 1H); 7.28-7.25 (m, 2H); 7.17 (s, 1H); 7.08 (m, 1H); 6.94 (app dt, J=1.2, 9.6 Hz, 1H), 6.87-6.82 (m, 1H); 5.99 (s, 1H), 5.34 (s, 2H), 5.20 (s, 2H); 4.43 (s, 2H); 2.29 (s, 3H). ES HRMS m/z 511.9672 (M+H C21H17Br2F2NO2 requires 511.9667).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067540B2
Source datasetuspto-grants-2006_06
ORD IDord-eb88ab64affc4f7dbca980dde6f4f0d1
Source noteuspto-grants-2006_06