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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258523Generated: November 2, 2026

Hydrogen Bromide → HCID 58137421, compound

https://huagongshe.com/reaction/1258523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantSodium NitriteHCID 23668193—
Reactant3-Amino-5-pentafluorosulfanylbenzoic acidHCID 58085706—
Catalystcopper(I) bromideHCID 24593—
ProductHCID 58137421HCID 58137421—

Reaction Steps

3-Amino-5-(pentafluorosulfanyl)benzoic acid (1.1 g; example 2a) was dissolved in 24% hydrogen bromide solution (40 ml). While stirring and cooling, sodium nitrite solution (290 mg dissolved in 20 ml of water) was added dropwise, in the course of which the temperature was not to exceed 5° C. On completion of formation of the diazonium salt, copper(I) bromide solution (720 mg dissolved in 15 ml of 48% hydrobromic acid) was cooled to 0° C. while stirring and the above diazonium salt solution was slowly added dropwise. Then the cooling bath was removed and the mixture was stirred at RT for 3 h. Thereafter, the reaction mixture was diluted with water and extracted repeatedly with EA. The combined EA phases were dried over magnesium sulfate, filtered and concentrated. The residue was dissolved in 500 ml of EA and filtered through a glass frit filled with a 10 cm silica gel layer. The filter layer was washed thoroughly with EA. The clear filtrate was concentrated, and solvent residues were drawn off under high vacuum. 800 mg of the title compound were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466169B2
Source datasetuspto-grants-2013_06
ORD IDord-ab184da08c42426598bff0dfa44a30a9
Source noteuspto-grants-2013_06