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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 365970Erstellt: 26. Oktober 2026

Sodium Hydroxide → (2-Aminophenyl)(cyclopropyl)methanone

https://huagongshe.com/reaction/365970

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
Edukt1-(o-Aminophenyl)-4-chloro-1-butanone hydrochlorideHCID 23293246—
KatalysatorTributylmethylammonium chlorideHCID 91822—
Lösungsmittel1,2-DichloroethaneHCID 11—
LösungsmittelDichloromethaneHCID 6344—
Produkt(2-Aminophenyl)(cyclopropyl)methanoneHCID 1093174170%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

A solution of 0.30 g (1.3 mmol) of 1-(o-aminophenyl)-4-chloro-1-butanone hydrochloride in 3 mL of methylene chloride and 3 mL of ethylene dichloride is treated with 1.2 g (3 mmol) of 10% sodium hydroxide solution and 0.05 g (0.2 mmol) of 75% aqueous methyl tributylammonium chloride and heated to 50° C. for about 5 hours. After cooling to room temperature, the phases are separated. The aqueous layer is extracted with methylene chloride. The combined organic extracts are washed with water and concentrated in vacuo to give 0.14 g (70% yield) of o-aminophenyl cyclopropyl ketone (mp 46-48° C.). The product is identified by NMR and MS analyses.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06127576
Quelldatensatzuspto-grants-2000_10
ORD IDord-c1e30ccef6c34666a0b9cc4091476cfe
Quellennotizuspto-grants-2000_10