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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782599Generated: October 30, 2026

Hydrochloric Acid → HCID 68808682, compound

https://huagongshe.com/reaction/1782599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium IodideHCID 5238—
ReactantSodiumHCID 5360545—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 68810143HCID 68810143—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 68808682HCID 6880868250%

Reaction Steps

A solution of N-pivaloyl-2-bromo-4-chloro-3-methoxyaniline (3.7 g, 1.2 mmol) in dioxane (35 mL) was treated with concentrated hydrochloric acid (35 mL) and the solution heated under reflux for 2 hours. After the solution was cooled the pH was adjusted to 10 by addition of sodium hyrdroxide (50% solution) and extracted with ethyl ether (2×50 mL). The combined extracts were washed with brine, dried (sodium sulfate) and concentrated. The crude aniline was dissolved in 2N hydrochloric acid and sodium nitrite (750 mg, 11 mmol) was added and the solution stirred for 20 minutes. This solution was poured into a vigorously stirred solution of sodium iodide (3.3 g, 22 mmol) in water (20 mL) and methylene chloride (30 mL) and stirred for 20 minutes. The solution was then extracted with methylene chloride (2×25 mL) and the combined extracts washed with brine, dried (sodium sulfate) and concentrated. The residue was purified by chromatography (hexanes) to give 2-bromo-4-chloro-1-iodo-3-methoxybenzene (1.5 g, 0.6 mmol): LC/MS (m/z=267).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498468B2
Source datasetuspto-grants-2009_03
ORD IDord-96567a27189e4f24a82283a924f1943f
Source noteuspto-grants-2009_03