Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368792Generated: October 30, 2026

Sodium hydride → HCID 67261866, compound

https://huagongshe.com/reaction/2368792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactantalpha-Bromo-o-fluorotolueneHCID 67968—
ReactantHCID 67260294HCID 67260294—
SolventDimethylformamideHCID 6228—
ProductHCID 67261866HCID 67261866—

Reaction Steps

To a suspension of 5-(2,4-difluorobenzyl)-3-iodopyridin-2(1H)-one 4 (5.58 g, 16.1 mmol) in anhydrous DMF (160 ml) was added at room temperature NaH (60% suspension in mineral oil, 0.71 g, 17.7 mmol). After the mixture was stirred for 15 min, o-fluorobenzyl bromide (2 ml, 16.1 mmol) was added to the mixture, which was stirred for 2 h at RT. The solvent was distilled off and the residue was dissolved in ethyl acetate (200 ml), washed with water (200 ml), brine (200 ml), and dried over anhydrous sodium sulfate and the solvent was distilled off. The residue was purified by flash chromatography on silica gel (hexanes:ethyl acetate, 80:20). Yield 6.61 g (90%). 1H NMR (CDCl3, 500 MHz): δ 7.80 (d, 1H, J=2.2 Hz), 7.55-7.51 (m, 1H), 7.32-7.27 (m, 2H), 7.13-7.04 (m, 3H), 6.86-6.79 (m, 2H), 5.14 (s, 2H), 3.64 (s, 2H). 13C NMR (CDCl3, 125 MHz): δ 162.4, 162.1, 160.5, 160.2, 159.1, 149.8, 136.5, 132.1, 131.1, 130.3, 124.6, 122.5, 121.9, 118.6, 115.4, 111.5, 104.2, 93.5, 48.5, 30.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703801B2
Source datasetuspto-grants-2014_04
ORD IDord-779a605cd1784d21a243461f1f998c1d
Source noteuspto-grants-2014_04