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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 727179Erstellt: 26. Oktober 2026

Methanol → 1-(3-Chlorophenyl)ethanone

https://huagongshe.com/reaction/727179

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktBenzonitrile, m-chloro-HCID 13015—
EduktHCID 178418573HCID 178418573—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(3-Chlorophenyl)ethanoneHCID 14933—

Reaktionsschritte

Under a nitrogen atmosphere, 36.7 mL (0.11 mole) of methylmagnesium bromide (3.0M in diethyl ether) is stirred, and a solution of 13.8 grams (0.10 mole) of 3-chlorobenzonitrile in 50 mL of dry tetrahydrofuran is added slowly dropwise. Upon completion of addition, the reaction mixture is warmed to reflux where it is stirred for about 18 hours. After this time the reaction mixture is cooled to ambient temperature, and about 40 mL of methanol is added dropwise. Upon completion of addition, the reaction mixture is stirred for two hours and then filtered. The filtrate is then stirred for about 18 hours with 35 grams of silica gel and 100 mL of water. The mixture is filtered, and the filtrate is diluted with ethyl acetate. The mixture is then washed with water, and the organic layer is dried with magnesium sulfate. The mixture is filtered, and the filtrate is concentrated under reduced pressure, yielding methyl 3-chlorophenyl ketone.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05712281
Quelldatensatzuspto-grants-1998_01
ORD IDord-1518c00294774bacbe3ba301d4199895
Quellennotizuspto-grants-1998_01