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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1515195Erstellt: 27. Oktober 2026

Iodine → (2-Aminophenyl)(1-methylpiperidin-4-yl)methanone

https://huagongshe.com/reaction/1515195

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktTetrahydrofuranHCID 8028—
Edukt2-AminobenzonitrileHCID 72913—
Edukt4-chloro-N-methylpiperidineHCID 79342—
EduktMagnesiumHCID 5462224—
EduktHCID 178478990HCID 178478990—
Produkt(2-Aminophenyl)(1-methylpiperidin-4-yl)methanoneHCID 214143857%

Reaktionsbedingungen

Temperatur45 °C

Reaktionsschritte

To a suspension of magnesium (1.8 g, 74 mmol) in dry THF (50 mL) in a flame-dried round bottomed flask under nitrogen was added 4-chloro-1-methylpiperidine (9.0 g, 68 mmol). A crystal of iodine and a catalytic amount of cyclohexylmagnesium chloride was added and the mixture was heated to reflux for 2 h. A gray precipitate formed, which was removed via vacuum filtration under a nitrogen atmosphere. To the filtrate was added a solution of 2-aminobenzonitrile (1.6 g, 14 mmol) in dry THF (15 mL). The stirred mixture was heated to 45° C. for 2 h. Ice was added and the reaction was quenched with 1 M sulfuric acid. The mixture was extracted with ethyl acetate and the acidic aqueous layer was then neutralized with 1 N sodium hydroxide, concentrated on a rotary evaporator and extracted with ethyl acetate. The combined organics were dried over sodium sulfate, filtered and concentrated to afford (2-aminophenyl)(1-methylpiperidin-4-yl)methanone as a yellow oil (1.0 g, 7%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08222263B2
Quelldatensatzuspto-grants-2012_07
ORD IDord-12e0fd4664a249cfbff59d2a38280fbb
Quellennotizuspto-grants-2012_07