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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629192Generated: October 29, 2026

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

https://huagongshe.com/reaction/629192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-6-nitrophenolHCID 13545453—
SolventDimethylformamideHCID 6228—
Product1-Bromo-2-methoxy-3-nitrobenzeneHCID 2250571396.4%

Reaction Steps

2-Bromo-6-nitrophenol (5.0 g, 22.9 mmol) was dissolved in DMF (3 mL), potassium carbonate (4.75 g, 34.4 mmol) was added and the reaction was stirred for 30 minutes. Next iodomethane (2.15 mL, 34.4 mmol) was added and the reaction was stirred overnight. The crude reaction was filtered, diluted with ethyl acetate and washed with brine (twice) and water (twice). The organic layer was dried over sodium sulfate, filtered and concentrated to provide 1-bromo-2-methoxy-3-nitrobenzene (5.12 g, 96%). LC retention time 0.92 [J].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315494B2
Source datasetuspto-grants-2016_04
ORD IDord-cb323723b0c04eb8bfe056acd9693d7e
Source noteuspto-grants-2016_04