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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426164Generated: October 30, 2026

Benzyl Bromide → 3-(Benzyloxy)-5-chloro-2-nitropyridine

https://huagongshe.com/reaction/1426164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantCesium carbonateHCID 10796—
Reactant5-Chloro-2-nitropyridin-3-olHCID 18765698—
SolventDimethylformamideHCID 6228—
Product3-(Benzyloxy)-5-chloro-2-nitropyridineHCID 6736943791%

Reaction Steps

1-(Bromomethyl)benzene (7.905 ml, 66.46 mmol) was added to a mixture of cesium carbonate (21.65 g, 66.46 mmol) and 5-chloro-2-nitropyridin-3-ol (11.6 g, 66.46 mmol) in DMF (50 mL). The reaction mixture was stirred overnight at ambient temperature, then partitioned between ethyl acetate and water, washed with water and brine, dried, and concentrated to afford 3-(benzyloxy)-5-chloro-2-nitropyridine (16.0 g, 91.0% yield) as a light yellow powder. 1H NMR (CDCl3) δ 5.25 (s, 2H), 7.41 (m, 5H), 7.53 (s, 1H), 8.04 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933077B2
Source datasetuspto-grants-2015_01
ORD IDord-7fa26f5191db426f9ea470beb4b8f849
Source noteuspto-grants-2015_01