HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 45656Erstellt: 25. Oktober 2026
Phenacyl bromide → 2-((2,4-Dichlorobenzyl)(methyl)amino)-1-phenylethanone
https://huagongshe.com/reaction/45656
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phenacyl bromide | HCID 6259 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Benzenemethanamine, 2,4-dichloro-N-methyl- | HCID 485424 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 2-((2,4-Dichlorobenzyl)(methyl)amino)-1-phenylethanone | HCID 22386899 | 90% |
Reaktionsschritte
Into a 50-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of 2-bromo-1-phenylethanone (1 g, 5.05 mmol, 1.00 equiv) in 1,4-dioxane (20 mL) and (2,4-dichlorophenyl)-N-methylmethanamine (1.1 g, 5.82 mmol, 1.15 equiv). Triethylamine (2 g, 19.80 mmol, 3.92 equiv) was added dropwise with stirring at 20° C. The resulting solution was stirred for 1 h at 20° C. in an oil bath. The solids were filtered out. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:50). This resulted in 1.4 g (90%) of the title compound as a yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08541448B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-0419d431c2244390b16ea63e4a4f739a |
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| Quellennotiz | uspto-grants-2013_09 |
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