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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 326249Erstellt: 24. Oktober 2026

Diethyl Ether → alpha-Phenyl-7-quinolinemethanol

https://huagongshe.com/de/reaction/326249

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
EduktBromobenzeneHCID 7961—
Edukt7-QuinolinecarboxaldehydeHCID 4712255—
EduktMagnesiumHCID 5462224—
LösungsmittelTetrahydrofuranHCID 8028—
Produktalpha-Phenyl-7-quinolinemethanolHCID 1996711326,6%

Reaktionsschritte

To a stirred mixture of 1.25 parts of magnesium, 14 parts of 1,1'-oxybisethane and 8 parts of bromobenzene was added a solution of 8 parts of intermediate 1, namely 7-quinolinecarboxaldehyde, in 72 parts of tetrahydrofuran, keeping the temperature between 0° C. and 5° C. After stirring for 12 hours at room temperature, the reaction mixture was poured into 300 parts of ice-water. The product was extracted with 1,1'-oxybisethane (3×70 parts). The combined extracts were dried, filtered and evaporated. The residue was purified by column chromatography (silica gel; CH2Cl2 /CH3OH 98:2). The eluent of the desired fraction was evaporated, yielding 3.2 parts (26.6%) of α-phenyl-7-quinolinemethanol; mp. 118° C. (interm. 2). In a similar manner there were also prepared the intermediates listed in Table 1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05268380
Quelldatensatzuspto-grants-1993_12
ORD IDord-ea6fb0e3e27a49cb991618f183d458d6
Quellennotizuspto-grants-1993_12