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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 513229Generated: October 30, 2026

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

https://huagongshe.com/reaction/513229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-6-nitrophenolHCID 13545453—
SolventAcetoneHCID 180—
Product1-Bromo-2-methoxy-3-nitrobenzeneHCID 22505713—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 2-Bromo-6-nitro-phenol (43.6 g, 0.2 mol), K2CO3 (82.9 g, 0.6 mol), acetone (600 mL) is stirred at 70° C. for 1 h. Then MeI (85.14 g, 0.6 mol) is slowly added to the reaction mixture and refluxed for 8 h. After reaction, filtered and the filtrate is extracted with ethyl acetate (3×1000 mL). The combined SnCl2 organic phase is washed with water and brine, dried over Na2SO4, concentrated in vacuo to obtain the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102684B2
Source datasetuspto-grants-2015_08
ORD IDord-fc21f8157e4c4316b1787911eafff502
Source noteuspto-grants-2015_08