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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735156Generated: October 30, 2026

Hydrochloric Acid → 858680-24-7

https://huagongshe.com/reaction/735156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium IodideHCID 4875—
ReactantSodium ThiosulfateHCID 24477—
Reactant2-Bromo-4-phenylanilineHCID 282627—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product858680-24-7HCID 68817951—

Reaction Conditions

Temperature15 °C

Reaction Steps

A solution of 7.3 g (29.4 mmol) of 3-bromobiphenyl-4-ylamine in 120 mL of acetic acid is mixed with 6 mL of concentrated hydrochloric acid at ambient temperature, cooled to 15° C., and stirred for 30 minutes. A solution of 2 g (28.9 mmol) of sodium nitrite in 7 mL of water is slowly added dropwise to this reaction mixture at 15° C. and stirred for 30 minutes. Then at 5° C., a solution of 5.4 g (32.5 mmol) of potassium iodide in 28 mL of water is slowly added dropwise and the mixture is stirred. After 30 minutes, 2.95 g of sodium thiosulfate is added and the mixture is stirred for a further 30 minutes. Then the reaction mixture is evaporated down and combined with water/ethyl acetate. The aqueous phase is again extracted with ethyl acetate, the combined aqueous phases are extracted once with water and dried over sodium sulfate. The purification is carried out by column chromatography on silica gel (eluant: petroleum ether). Yield: 6.6 g (85% of theory); C12H8BrI (M=359.00); calc.: molecular ion peak (M)+: 358/360 (Br); found: molecular ion peak (M)+: 358/360 (Br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592373B2
Source datasetuspto-grants-2009_09
ORD IDord-a98ccf91f355463eabeb6886c0480318
Source noteuspto-grants-2009_09