Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1033412Erstellt: 26. Oktober 2026

Diethyl Ether → Stannane, trimethyl(4-methylphenyl)-

https://huagongshe.com/reaction/1033412

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
EduktDi-p-tolylHCID 11941—
EduktTrimethyltin chlorideHCID 14016—
EduktAmmonium ChlorideHCID 25517—
EduktHCID 178418370HCID 178418370—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktStannane, trimethyl(4-methylphenyl)-HCID 617834100%

Reaktionsschritte

41.4L of 1.0 M p-tolylmagnesium bromide in diethyl ether (41.4 mol) was added dropwise, maintaining the temperature below -5° C., over 4 hours to a solution of 546 g (2.79 mol) of trimethyltin chloride in tetrahydrofuran (4L) under nitrogen at -10 C. The suspension was allowed to warm slowly to room temperature over 12 h then saturated ammonium chloride solution (1L) was added followed by sufficient water (approximately 1L) to dissolve the precipitate. The solution was extracted with ether-hexane (1:1) (1×4L, 3×2L). The combined organic phases were washed with brine, dried over magnesium sulfate and the solvents removed under vacuum. Purification by flash chromatography on silica gel eluting with hexane/ethyl acetate (95:5) gave a pale yellow oil containing white crystals of 4,4'-dimethylbiphenyl which were removed by filtration to leave 711.3 g (100%) of product. 1H NMR (300MHz,CDCl3): 0.30 (s,9H), 2.34 (s,3 H), 7.19 (d,7.7Hz,2H), 7.40 (d,7.7Hz,2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05310737
Quelldatensatzuspto-grants-1994_05
ORD IDord-ae282d93c464437792eb653292e5b568
Quellennotizuspto-grants-1994_05