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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434158Generated: October 31, 2026

Water → HCID 21914155, compound

https://huagongshe.com/reaction/434158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Bromo-4-nitroanisoleHCID 78870—
Reactant4-Aminomethylphenylboronic acid hydrochlorideHCID 2734311—
ReactantSodiumHCID 5360545—
CatalystTriphenylphosphineHCID 11776—
Catalystpalladium(II) acetateHCID 167845—
Solvent1-PropanolHCID 1031—
ProductHCID 21914155HCID 2191415571.2%

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of 2-bromo-4-nitroanisole (5.80 g, 25.0 mmol) and 4-(aminomethyl)phenylboronic acid hydrochloride (4.96 g, 26.6 mmol) was slurried in 1-propanol (50 mL) under nitrogen. Triphenylphosphine (315 mg, 1.20 mmol) and palladium(II)acetate (90 mg, 0.40 mmol) were added, followed by 2.0N sodium carabonate (33 mL, 66 mmol). The mixture was heated at 95° C. (oil bath) under nitrogen for 3 hours, at which time the reaction was judged to be complete by TLC. Water (25 mL) was added and the mixture was stirred open to air for 2 hours at room temperature. The mixture was extracted with ethyl acetate (100 mL, 2×50 mL) and the combined extracts were washed with sodium bicarbonate (25 mL) and brine (25 mL). The solution was dried with sodium sulfate, and concentrated to an oil which was purified by flash chromatography on silica gel (100 g) eluting with 0-4% methanol/0,5% triethylamine/dichloromethane. Pure fractions were combined and concentrated to give 2-(4-aminomethylphenyl)-4-nitroanisole (4.6 g) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06670376B1
Source datasetuspto-grants-2003_12
ORD IDord-68594837b77f414fb89ecb6647f880cf
Source noteuspto-grants-2003_12