Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1070988Erstellt: 25. Oktober 2026

2-Methylindole → HCID 22398526, Verbindung

https://huagongshe.com/reaction/1070988

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-MethylindoleHCID 7224—
Edukt4-(5-Fluoro-2-methoxyphenyl)-4-methylpentan-2-oneHCID 22284922—
EduktPotassium tert-butoxideHCID 23665647—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 22398526HCID 2239852631,2%

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

To a solution of 2-methylindole (130 mg) in THF (2 mL) stirred under argon cooled on dry ice/acetone was added n-butyl lithium (2M in pentane, 1.6 mL). After 2 minutes, potassium tert-butoxide (1M in THF, 2 mL) was added and the mixture was allowed to warm to approximately −20° C. After 5 minutes, precipitate was noted and the mixture was cooled to −70° C. 4-(5-Fluoro-2-methoxyphenyl)-4-methylpentan-2-one (Example 17) (440 mg) in THF (1.5 mL) was added all at once. The cooling bath was removed and the mixture was stirred for 10 minutes and then quenched with EtOH (0.5 mL). The mixture was diluted with EtOAc, washed with water, dried, filtered, and evaporated. Chromatography over silica gel (EtOAc-hexanes (1:9)) gave product which solidified on trituration with hexanes-ether. The solid was recrystallized from ether-hexanes, collected by filtration and dried under vacuum to give 0.11 g of the title compound, m.p. 118° C.-120° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06903215B2
Quelldatensatzuspto-grants-2005_06
ORD IDord-9e6c33ba1522492789ec02b6cd857878
Quellennotizuspto-grants-2005_06