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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057111Generated: November 3, 2026

Sodium Thiosulfate → 4-Bromo-3-fluoro-2-methylaniline

https://huagongshe.com/reaction/1057111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantN-bromobutanimideHCID 67184—
Reactant3-Fluoro-2-methylanilineHCID 285553—
SolventAcetonitrileHCID 6342—
Product4-Bromo-3-fluoro-2-methylanilineHCID 15746684—

Reaction Steps

To a solution of 3-fluoro-2-methylaniline (20 g, 0.16 mol) in CH3CN (500 mL) was added NBS (31.3 g, 0.176 mol) in portions at 10° C. The resulting mixture was stirred at room temperature for 30 minutes. Upon completion, saturated Na2S2O3 (500 mL) was added slowly into the reaction mixture at 10° C. The organic layer was separated, and the aqueous layer was extracted with EtOAc. The combined organic layers were dried over Na2SO4 and concentrated in vacuo. The residue was washed with petroleum ether affording the title compound (20 g), which was used in the next step without further purification. 1H NMR (300 MHz, DMSO-d6): δ 7.08 (t, 1H), 6.40 (dd, 1H), 5.35 (br, 2H), 1.98 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399646B2
Source datasetuspto-grants-2016_07
ORD IDord-f3174abf9bc540dcb332f058c038c964
Source noteuspto-grants-2016_07