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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407021Generated: October 28, 2026

Hydrochloric Acid → 4-Bromo-3-methoxybenzonitrile

https://huagongshe.com/reaction/2407021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CyanideHCID 9032—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-3-methoxyanilineHCID 7018254—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 178418546HCID 178418546—
SolventWaterHCID 962—
Product4-Bromo-3-methoxybenzonitrileHCID 2259118140.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-bromo-3-methoxyaniline (4 g, 19.8 mmol) in water (22 mL) was added concentrated HCl (7 mL). After cooling to 0° C., a solution of sodium nitrite (1.5 g, 22 mmol) in water (5 mL) was added dropwise. The resulting mixture was stirred at 0° C. for 30 min. After neutralizing with solid potassium carbonate, the reaction mixture was added to a mixture of copper (I) cyanide (2.13 g, 23.8 mmol) and potassium cyanide (3.2 g, 50 mmol) in water (22 mL) at 70° C. The reaction mixture was stirred at 70° C. for 1 h. After cooling to room temperature, the reaction was extracted with toluene (100 mL*4). The combined extracts were dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified by silica gel chromatography to give 4-bromo-3-methoxybenzonitrile (1.7 g) as a yellow solid. 1HNMR (400 MHz, CDCl3) δ 7.64 (d, J=8.4 Hz, 1H), 7.14 (dd, J=8.0, 1.6 Hz, 1H), 7.09-7.10 (m, 1H), 3.87 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809342B2
Source datasetuspto-grants-2014_08
ORD IDord-fa2ba464c5f84ea0bc758217b376ce92
Source noteuspto-grants-2014_08