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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041818Generated: November 2, 2026

Hydrochloric Acid → HCID 12595487, compound

https://huagongshe.com/reaction/2041818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium IodideHCID 4875—
Reactant2'-amino-p-terphenylHCID 12595486—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 23703134HCID 23703134—
SolventDichloromethaneHCID 6344—
ProductHCID 12595487HCID 1259548767%

Reaction Conditions

Temperature80 °C

Reaction Steps

3N hydrochloric acid (300 milliliters) was added to 2,5-diphenylanilin obtained in the foregoing (25 g, 101.91 mmol, 1.0 equivalent), and the mixture was stirred at 80° C. for 2.5 hours. After that, the mixture was cooled to room temperature. After that, the mixture was further cooled to 5° C. While the temperature of the mixture was kept at 10° C. or lower (5 to 8° C.), an aqueous solution of sodium nitrite (NaNO2: 8.43 g, 122.29 mmol, 1.2 equivalents, H2O: 60 milliliters) was slowly added to the mixture, and the whole was stirred for 0.5 hour. The reaction liquid was dropped into an aqueous solution of potassium iodide (KI: 60.9 g, 366.87 mmol, 3.6 equivalents, H2O: 180 milliliters). An appropriate amount of methylene chloride was further added to the mixture so that a reaction was completed, and the whole was stirred for 0.75 hour at room temperature. Sodium hydrogen dithionite was added to the reaction liquid until the color of the reaction liquid was turned into a yellow color. After that, the mixture was stirred for 0.5 hour, and the organic layer of the resultant reaction liquid was extracted. The extracted organic layer was washed with a saturated salt solution, dried with anhydrous sodium sulfate, and concentrated. The resultant residue was purified by short column chromatography (methylene chloride) and silica gel chromatography (methylene chloride:hexane=1:1→2:1), and the purified residue was dried, whereby a pale pink solid was obtained (24.35 g, yield: 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586199B2
Source datasetuspto-grants-2013_11
ORD IDord-f7713d90277c4658b7c6b088a0d569a4
Source noteuspto-grants-2013_11