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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575790Generated: October 30, 2026

Ethanol → 3-Bromo-5-(2,4-difluorophenoxy)aniline

https://huagongshe.com/reaction/575790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(3-Bromo-5-nitrophenoxy)-2,4-difluorobenzeneHCID 118021815—
CatalystIronHCID 23925—
SolventTetrahydrofuranHCID 8028—
Product3-Bromo-5-(2,4-difluorophenoxy)anilineHCID 118021910100%

Reaction Steps

A mixture of 1-(3-bromo-5-nitrophenoxy)-2,4-difluorobenzene (54 mg, 0.16 mmol), ammonium chloride (18 mg, 0.32 mmol), and iron powder (45 mg, 0.80 mmol) suspended in THF (300 uL), water (100 uL) and ethanol (300 uL) was heated to 100° C. using microwave irradiation (normal) for 3 h. The crude reaction mixture was filtered through a short plug of celite; the celite plug was washed with MeOH (˜5 mL). The resulting filtrate was concentrated in vacuo. The resulting residue was diluted with EtOAc (50 ml) and washed with saturated bicarbonate solution (aq), dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The crude solid was purified by silica gel column chromatography using a gradient of EtOAc (5 to 20%) in hexanes to afford the title compound (48 mg, 100%) as a yellow solid. LCMS (M+H)+=301.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034900B2
Source datasetuspto-grants-2015_05
ORD IDord-5e0bcb8ddbf143418b7b9399c9e5f58e
Source noteuspto-grants-2015_05