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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 562866Generated: October 25, 2026

Methyl iodide → 2-Chloro-1-methoxy-3-nitrobenzene

https://huagongshe.com/reaction/562866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant2-NitrophenolHCID 6947—
ReactantCesium carbonateHCID 10796—
ReactantPhenol, 2-chloro-3-nitro-HCID 3013917—
SolventDimethylformamideHCID 6228—
Product2-Chloro-1-methoxy-3-nitrobenzeneHCID 1241182798%

Reaction Steps

The nitrophenol starting material C2 (1.3 g; 7.49 mmol) was dissolved in DMF (10 mL) and to this solution was added ground cesium carbonate (2.92 g; 8.96 mmol), followed by MeI (1.4 mL; 22.5 mmol). The mixture was stirred at room temperature overnight. The DMF was evaporated in vacuo and the residue taken up in ether (150 mL), washed with water (150 mL), brine (4×100 mL), and then dried over (MgSO4). The organic phase was filtered and evaporated to afford the crude 2-chloro-3-nitroanisole C3 (98%; 1.38 g) as an orange solid. Homogeneity by HPLC (TFA) @ 220 nm: 93%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067438B2
Source datasetuspto-grants-2011_11
ORD IDord-4c8d32eb7429488982b09ad613473bcd
Source noteuspto-grants-2011_11