Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417527Generated: November 1, 2026

Hydrogen Bromide → 2,5-Bis(trifluoromethyl)bromobenzene

https://huagongshe.com/reaction/1417527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant2,5-Bis(trifluoromethyl)anilineHCID 719818—
ReactantSodium NitriteHCID 23668193—
CatalystCopperHCID 23978—
SolventWaterHCID 962—
Product2,5-Bis(trifluoromethyl)bromobenzeneHCID 2734763—

Reaction Steps

A suspension of the HBr salt of 2,5-bis-trifluoromethylaniline (1.0 gm, 4.4 mmol) was prepared by addition of 48% HBr (3 gm, 17.5 mmol) and 5 mL of water. This was cooled in an ice bath while a solution of sodium nitrite (335 mg, 4.8 mmol) in 1 mL of water was added dropwise. The reaction was stirred a farther 0.5 hr at which time copper powder (1 gm) and another 3 gm portion of 48% HBr were added. The reaction was heated to reflux and after 10 min the distillate was collected until no organic material was evident with the water. The distillate was extracted twice with ether and the ether layers were washed with brine, dried over sodium sulfate, combined and evaporated. The residue was purified by flash chromatography (5% ethyl acetate/hexanes) to afford the title compound as an oil. NMR (CDCl3): δ 7.68 (d, 1H, J=8 Hz), 7.81 (d, 1H, J=8 Hz), 7.96 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05877191
Source datasetuspto-grants-1999_03
ORD IDord-f890d777f47742b6a857b311e422bd22
Source noteuspto-grants-1999_03