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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869076Generated: October 30, 2026

4-Methoxybenzyl bromide → 3-chloro-1-(4-methoxy-benzyl)-5-nitro-1H-pyridin-2-one

https://huagongshe.com/reaction/869076

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzyl bromideHCID 165021—
ReactantHCID 178526838HCID 178526838—
Product3-chloro-1-(4-methoxy-benzyl)-5-nitro-1H-pyridin-2-oneHCID 86703125—

Reaction Steps

The title compound was prepared in analogy to the procedure described for step W2 but using 3-chloro-2-hydroxy-5-nitropyridine and 4-methoxybenzyl bromide. The reaction was quenched with a saturated aqueous solution of sodium bicarbonate. The residue was purified by trituration in EtOAc. tR: 0.98 min (LC-MS 4); ESI-MS: 295.2 [M+H]+ (LC-MS 4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969341B2
Source datasetuspto-grants-2015_03
ORD IDord-412f86190428432b81e7fed2a2c315a7
Source noteuspto-grants-2015_03