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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21563Erstellt: 24. Oktober 2026

Hexane → 4-(3-Furyl)-7-methylcoumarin

https://huagongshe.com/de/reaction/21563

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexaneHCID 8058—
EduktTrimethyl borateHCID 8470—
Edukt3-BromofuranHCID 89164—
Edukt7-Methyl-2-oxo-2H-chromen-4-YL trifluoromethanesulfonateHCID 23370238—
EduktButyllithiumHCID 178418339—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(3-Furyl)-7-methylcoumarinHCID 2337019075,7%

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

To a solution of 3-bromofuran (2.3 g, 16.1 mmol) in dry Et2O (146 ml) was added at -78° C. n-BuLi in hexane (6.42 ml, 16.1 mmol, 2.5M). The resulting solution was stirred for 20 min, then (MeO)3B (1.82 ml, 16.1 mmol) was added dropwise and after 20 min., a mixture of the triflate from Step 1 (4.50 g, 14.6 mmol) and (PPh3)4Pd (1.69 g, 1.46 mmol) in THF (60 ml) and H2O (10 ml) was added. The cooling bath was removed and the resulting mixture was heated to 65° C. for 1.75 h. The solvent was evaporated and H2O was added followed by extraction with EtOAc (3×50 ml). The combined organic phases were washed with brine, dried over MgSO4 and evaporated. Purification by flash chromatography (toluene:(2-10% EtOAc)) gave 2.5 g of the title compound, m.p. 160°-162° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05424320
Quelldatensatzuspto-grants-1995_06
ORD IDord-e8506f15126a449896a0839e0d8b9da3
Quellennotizuspto-grants-1995_06