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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 63080Erstellt: 24. Oktober 2026

Iodobenzene → 5-phenoxy-3,4-dihydronaphthalen-1(2H)-one

https://huagongshe.com/de/reaction/63080

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodobenzeneHCID 11575—
EduktSodium hydrideHCID 24758—
EduktEthanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]-HCID 112414—
Edukt5-Hydroxy-1-tetraloneHCID 119921—
KatalysatorCuprous chlorideHCID 62652—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt5-phenoxy-3,4-dihydronaphthalen-1(2H)-oneHCID 1072862518%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To a solution of 5-hydroxy-1-tetralone (4.5 g, 28.0 mmol) and iodobenzene (24.0 g, 168.0 mmol) in DMF (50 mL) was added NaH (1.2 g, 30.0 mmol) at room temperature. The mixture was heated to 50° C. until the solid was dissolved and then cooled. To the mixture was added CuCl (2.8 g, 28.0 mmol); followed by tris(dioxa 3,6-heptyl)amine (2.7 g, 8.4 mmol). The mixture was heated at 145° C. overnight. The reaction was diluted with water, extracted with EtOAc, washed with brine, dried (Na2SO4), and concentrated. Purification by silica gel chromatography (20:1 PE/EtOAc) gave 1.2 g (18%) of the title compound as a yellow oil. [M+H] calc'd for C16H14O2, 239; found 239.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09447045B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-328b236c2f914b0ca6c088a7a6bd926a
Quellennotizuspto-grants-2016_09