HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491424Generated: November 1, 2026
2,6-Dibromoaniline → HCID 57678304, compound
https://huagongshe.com/reaction/491424
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Dibromoaniline | HCID 69098 | — |
| Reactant | 4-tert-Butylbenzoyl chloride | HCID 74372 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 57678304 | HCID 57678304 | 81.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07531542B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-f6ae222480e640beabfa5ab9d46c5ab1 |
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| Source note | uspto-grants-2009_05 |
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