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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717648Generated: November 4, 2026

Methanol → 4-Bromo-2-methoxybenzonitrile

https://huagongshe.com/reaction/1717648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-2-fluorobenzonitrileHCID 736029—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product4-Bromo-2-methoxybenzonitrileHCID 2234670295.6%

Reaction Conditions

Temperature55 °C

Reaction Steps

A mixture of 4-bromo-2-fluoro-benzonitrile (15.0 g, 75.0 mmol), methanol (30.4 mL, 350 mmol) and potassium carbonate (31.1 g, 225 mmol) in DMF (150 mL) was stirred under argon at 55° C. overnight. At this point TLC (100% methylene chloride) revealed no starting material, and the reaction mixture was poured into ether (300 mL) and water (150 mL). The layers were separated, and the organic layer was washed with water (150 mL) and brine (50 mL), dried over Mg2SO4, filtrated, and concentrated under reduced pressure, providing (15.2 g. 95.5%) of 4-bromo-2-methoxy-benzonitrile as a white solid. 1H-NMR (CDCl3) δ 7.41 (d, J=8.1 Hz, 1H), 7.16 (dd, J=8.1, 1,6 Hz, 1H), 7.13 (d, J=1.6 Hz, 1H), 3.93 (s, 3H); MS GC-MS (M+=211; RT=6.15 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803956B2
Source datasetuspto-grants-2010_09
ORD IDord-37c03fc7972948809d4e11f747a23dec
Source noteuspto-grants-2010_09