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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 562863Generated: October 25, 2026

Methyl iodide → 2-Bromo-3-nitroanisole

https://huagongshe.com/reaction/562863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant2-NitrophenolHCID 6947—
ReactantCesium carbonateHCID 10796—
Reactant2-Bromo-3-nitrophenolHCID 8167254—
SolventDimethylformamideHCID 6228—
Product2-Bromo-3-nitroanisoleHCID 1775029994%

Reaction Steps

The nitrophenol starting material B2 (3.1 g; 14.2 mmol) was dissolved in DMF (20 mL) and to the solution was added ground cesium carbonate (5.58 g; 17.1 mmol) followed by MeI (2.6 mL; 42.5 mmol). The mixture was stirred at room temperature overnight. The DMF was evaporated, the residue taken up in ether (1×200 mL), washed with water (1×200 mL), brine (4×100 mL), dried (MgSO4), filtered and evaporated to afford the crude 2-bromo-3-nitroanisole B3 (94%; 3.1 g) as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067438B2
Source datasetuspto-grants-2011_11
ORD IDord-62fe4f27dc5a4e17be77b4c04519d7bf
Source noteuspto-grants-2011_11