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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7891Erstellt: 24. Oktober 2026

Tetramethyltin → 2-Butyl-6-fluoro-5-methoxy-4-methyl-1-indanone

https://huagongshe.com/de/reaction/7891

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetramethyltinHCID 11661—
EduktTriphenylphosphineHCID 11776—
EduktLithium ChlorideHCID 433294—
Edukt4-Bromo-2-butyl-6-fluoro-5-methoxy-1-indanoneHCID 21990906—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-Butyl-6-fluoro-5-methoxy-4-methyl-1-indanoneHCID 2199086324,5%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of 4-bromo-2-butyl-6-fluoro-5-methoxy-1-indanone (1.86 g, 5.94 mmol), bis(triphenylphosphine)palladium(II) chloride (208 mg, 0.297 mmol), tetramethyltin (0.989 mL, 7.128 mmol), triphenylphosphine (156 mg, 0.594 mmol), lithium chloride (504 mg, 11.88 mmol), and anhydrous N,N-dimethyl-formamide (11.9 mL) was placed under a nitrogen atmosphere, stirred, and heated in an oil bath at 100° C. for 22 hours. After cooling to room temperature, the mixture was evaporated under vacuum. The residue in EtOAc (150 mL) was washed with water (4×100 mL) and brine (50 mL), dried over MgSO4, filtered, and evaporated under vacuum to an oil (2.15 g). The crude product was purified by chromatography on EM silica gel 60 (2.5×29 cm column), eluting with CH2Cl2 (50 mL fore-run followed by 8 mL fractions). Fractions 20-28 were combined and evaporated under vacuum to provide 2-butyl-6-fluoro-5-methoxy-4-methyl-1-indanone (365 mg) as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087599B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-270913168eb241f99a23be25455ccdcc
Quellennotizuspto-grants-2006_08