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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056098Generated: November 2, 2026

2-Bromo-3-fluoro-6-nitroaniline → 3-Bromo-4-fluorobenzene-1,2-diamine

https://huagongshe.com/reaction/1056098

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-3-fluoro-6-nitroanilineHCID 19429780—
CatalystPlatinumHCID 23939—
SolventEthanolHCID 702—
Product3-Bromo-4-fluorobenzene-1,2-diamineHCID 53395390—

Reaction Steps

A 500 mL round-bottomed flask containing Pt/C (5%, 6.00 g, 1.54 mmol) and 2-bromo-3-fluoro-6-nitroaniline (600b) (20.85 g, 89 mmol) were treated with EtOH (250 mL) and stirred under an atmosphere of H2 (balloon) for 22 h. LC-MS indicated ca. 35% conversion to the desired material (M+1=204.9/206.9). Another balloon of H2 was added and it was stirred for another 16 h resulting in >90% conversion to the desired product (M+1=204.9/207.1) by LC-MS. The suspension was filtered through a plug of Celite washing with EtOH and concentrated affording crude 3-bromo-4-fluorobenzene-1,2-diamine (18 g, 88 mmol, 99% yield) as a black/purple viscous oil. 1H NMR (400 MHz, CDCl3) δ ppm 6.60 (1H, dd, J=8.5, 5.2 Hz), 6.42-6.50 (1H, m). 19F NMR (376 MHz, CDCl3) δ ppm −116.48 (1F, s). m/z (ESI, +ve ion) 204.9/206.9 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394297B2
Source datasetuspto-grants-2016_07
ORD IDord-f5fe1325420149b1a47b1827ab20498c
Source noteuspto-grants-2016_07