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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831897Generated: October 30, 2026

Benzyl Bromide → HCID 22050336, compound

https://huagongshe.com/reaction/1831897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantHCID 54724175HCID 54724175—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 22050336HCID 22050336—

Reaction Steps

A mixture of 1-(2,6-dichlorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one (0.125 g, 0.46 mmol) and benzylbromide (0.1 mL) in DMF (2.5 mL) was stirred at room temperature for 16 h. The reaction mixture was diluted with water (10.0 mL) and extracted with EtOAc (2×20 mL). The combined organic extracts were washed with water, dried (Na2SO4), filtered, concentrated under reduced pressure and the resulting material was purified by silica gel flash chromatography using 25% EtOAc in hexanes to afford the title compound (0.11 g) as a pale yellow syrup: 1H-NMR (CD3OD) δ: 7.61 (m, 2H), 7.55-7.3 (m, 6H), 6.23 (d, 1H, J=2.0 Hz), 6.01 (d, 1H, J=2.0 Hz), 5.12 (s, 2H), and 1.93 (s, 3H); ES-MS m/z=360 (MH+); HR-MS, m/z calc C19H16NO2Cl2, 360.0553, found 360.0569.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067540B2
Source datasetuspto-grants-2006_06
ORD IDord-7c1e0eaff3414355b90a5e1fdee9af08
Source noteuspto-grants-2006_06