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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenacyl bromideHCID 6259—
EduktTriethylamineHCID 8471—
EduktBenzenemethanamine, 2,4-dichloro-N-methyl-HCID 485424—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt2-((2,4-Dichlorobenzyl)(methyl)amino)-1-phenylethanoneHCID 2238689990%

Reaktionsbedingungen

Temperatur20 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541448B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-0419d431c2244390b16ea63e4a4f739a
Quellennotizuspto-grants-2013_09