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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491424Generated: November 1, 2026

2,6-Dibromoaniline → HCID 57678304, compound

https://huagongshe.com/reaction/491424

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DibromoanilineHCID 69098—
Reactant4-tert-Butylbenzoyl chlorideHCID 74372—
ReactantDiisopropylethylamineHCID 81531—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 57678304HCID 5767830481.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

2,6-Dibromoaniline (1.0 g, 3.98 mmol) was dissolved in dioxane (20 mL) and treated with diisopropylethylamine (1.39 mL, 7.96 mmol) followed by 4-tert-Butylbenzoyl chloride (1.70 g, 7.96 mmol). The solution was warmed to 60° C. and stirred overnight. The mixture was concentrated under reduced pressure and the residue was re-dissolved in ethyl acetate (50 mL). The organic solution was washed with 10% HCl (2×50 mL), saturated sodium carbonate (50 mL) and saturated sodium chloride (50 mL). The organic layer was dried (magnesium sulfate), filtered, and concentrated under reduced pressure. The residue was purified by flash silica gel chromatography, eluting with 20% acetone/hexane to yield 1.33 g (81%) of product. MS (ESI) m/z 409.9772; HPLC Method B, purity 92.3% at 210-370 nm, 10.4 min.; 89.7% at 232 nm, 10.4 min.; HRMS: calcd for C17H17Br2NO+H+, 409.97496; found (ESI, [M+H]+), 409.9772.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531542B2
Source datasetuspto-grants-2009_05
ORD IDord-f6ae222480e640beabfa5ab9d46c5ab1
Source noteuspto-grants-2009_05