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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1022577Erstellt: 27. Oktober 2026

Diethyl Ether → 1-(3,4-Dichlorophenyl)-2-methoxyethanone

https://huagongshe.com/reaction/1022577

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
EduktMethoxyacetonitrileHCID 74442—
EduktMagnesiumHCID 5462224—
EduktHCID 178478192HCID 178478192—
Lösungsmittel4-Bromo-1,2-dichlorobenzeneHCID 29013—
Produkt1-(3,4-Dichlorophenyl)-2-methoxyethanoneHCID 20255641—
ProduktHCID 178478192HCID 178478192—

Reaktionsschritte

A solution (about 100 mL) of 3,4-dichlorophenylmagnesium bromide in diethyl ether was prepared from a mixture of magnesium (flakes) (2.07 g) in diethyl ether (100 mL) and 1-bromo-3,4-dichlorobenzene (17.5 g). A solution of methoxyacetonitrile (5.0 g) in diethyl ether (10 mL) was added dropwise to a solution of 3,4-dichlorophenylmagnesium bromide in diethyl ether under ice-cooling, and the resulting mixture was stirred under ice-cooling for 20 min. The reaction mixture was quenched with water, the mixture was acidified with 1 N hydrochloric acid, and the mixture was stirred under ice-cooling for 15 min. The reaction mixture was extracted with ethyl acetate, the organic layer was washed with water and brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated to give a pale-yellow oil. The oil was purified by silica gel column chromatography (eluent; hexane:ethyl acetate (19:1-1:1)) to give the title compound (10.5 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08722662B2
Quelldatensatzuspto-grants-2014_05
ORD IDord-b6a355e289e34e41aa931d4762177826
Quellennotizuspto-grants-2014_05