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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 964565Erstellt: 24. Oktober 2026

Dibenzofuran → Dibenzofuran, 4-methyl-

https://huagongshe.com/de/reaction/964565

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDibenzofuranHCID 568—
EduktDimethyl SulfateHCID 6497—
EduktAmmonium ChlorideHCID 25517—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktDibenzofuran, 4-methyl-HCID 43489100,2%

Reaktionsschritte

Dibenzofuran (26.94 g, 160 mmol) was dissolved in dry THF (500 ml) and cooled to -78° C. n-Butyl lithium (1.6M in hexane, 200 ml, 320 mmol) was added in portions over 30 mins. and the solution was allowed to warm to room temperature over 2.5 hours. The solution was recooled to -70° C. and a mixture of dimethyl sulphate (32 ml, 340 mmol) in dry THF (100 ml) was added dropwise. Once the addition was complete, the reaction was allowed to warm to room temperature, stirred for 18 hours and poured onto saturated ammonium chloride solution (400 ml). The phases were separated and the aqueous extracted twice with ether. The combined organic phases were dried (MgSO4) and evaporated in vacuo. Chromatography on silica (eluting with 40-60 petrol) gave the pure product as a clear oil (29.2 g, 100%) δH [2H6 ]-DMSO 8.1 (1H, d), 7.9 (1H, d), 7.7 (1H, d),7.5 (1H, t), 7.4 (1H, t), 7.25 (2H, m), 2.55 (3H, s).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05770598
Quelldatensatzuspto-grants-1998_06
ORD IDord-31779468f8784f4498be2fec604b723d
Quellennotizuspto-grants-1998_06