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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82044Generated: October 26, 2026

Triethylamine → 4-Bromo-N-(3-iodo-phenyl)-butyramide

https://huagongshe.com/reaction/82044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-IodoanilineHCID 12271—
Reactant4-Bromobutyryl chlorideHCID 70225—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventCyclohexaneHCID 8078—
Product4-Bromo-N-(3-iodo-phenyl)-butyramideHCID 8667817764%

Reaction Steps

To a solution of 3-iodoaniline (1.5 g, 6.85 mmol) and triethylamine (1.34 mL, 9.59 mmol) in dichloromethane (28 mL) at 0° C. was added dropwise 4-bromobutyryl chloride (0.99 mL, 8.56 mmol). The reaction mixture was then stirred at room temperature overnight. The organic extract was washed with an aqueous 1M HCl solution, aqueous 1M NaOH solution and brine, dried (Na2SO4), filtered, concentrated under vacuum. The crude residue was purified by silica gel column chromatography using a gradient of EtOAc (0-15%) in cyclohexane to yield a sticky solid. Trituration in a mixture of cyclohexane and ether and then filtration give the title compound as a solid (1.61 g, 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846712B2
Source datasetuspto-grants-2014_09
ORD IDord-f7871a57384f4a538967d51a3894c02f
Source noteuspto-grants-2014_09