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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947929Generated: November 2, 2026

Bromine → 4-Bromo-3-fluoro-2-methoxyaniline

https://huagongshe.com/reaction/1947929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant3-Fluoro-2-methoxyanilineHCID 581109—
SolventAcetic AcidHCID 176—
Product4-Bromo-3-fluoro-2-methoxyanilineHCID 57955529—

Reaction Steps

To a solution of 2-methoxy-3-fluoroaniline (Compound 1471, 7.70 g, 54.6 mmol) in AcOH (45.0 mL) was added a solution of bromine (6.98 g, 43.6 mmol) in AcOH (45.0 mL) dropwise. The reaction mixture was stirred at rt for 30 minutes. The resulting solid was filtered and washed with acetic acid to give the HBr salt of the desired product. The solid was dissolved in water (15 mL), basified by addition of KOH, and extracted with EtOAc (20 mL). The organic layer was dried over Na2SO4 and concentrated under reduced pressure to give a white solid. The crude material was purified by silica gel chromatography on an ISCO combi-flash Rf system using Heptane/EtOAc (100:0→70:30) as eluent to yield the desired product as a white solid, 6.536 mg (54% yield). 1H NMR (CDCl3, 400 MHz): δ=3.93 (d, J=1.52 Hz, 3H), 6.42 (dd, J=8.84, 1.77 Hz, 1H), 7.01 (dd, J=8.72, 6.95 Hz, 1H). MS (ES+): m/z 221.98 [MH+] (TOF, polar).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399433B2
Source datasetuspto-grants-2013_03
ORD IDord-e020b11bd4b9449f9550039a5c6f4cd5
Source noteuspto-grants-2013_03