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

HRID 1080722

Reaktionsgleichung

Reaktionsgleichung von HRID 1080722
[C:1]1([CH3:9])[CH:6]=[CH:5][C:4]([Mg]Br)=[CH:3][CH:2]=1.C(OCC)C.[CH3:15][Sn:16](Cl)([CH3:18])[CH3:17].[Cl-].[NH4+].CC1C=CC(C2C=CC(C)=CC=2)=CC=1>O1CCCC1.O>[CH3:9][C:1]1[CH:6]=[CH:5][C:4]([Sn:16]([CH3:18])([CH3:17])[CH3:15])=[CH:3][CH:2]=1

Komponenten

8

Edukt 5

HCID 3283Diethyl EtherHCID 11941Di-p-tolylHCID 14016Trimethyltin chlorideHCID 25517Ammonium ChlorideHCID 178418370HCID 178418370, Verbindung

Produkt 1

HCID 617834Stannane, trimethyl(4-methylphenyl)-Ausbeute 100 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

41.4 L of 1.0M 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 (4 L) under nitrogen at -10° C. The suspension was allowed to warm slowly to room temperature over 12 h then saturated ammonium chloride solution (1 L) was added followed by sufficient water (approximately 1 L) to dissolve the precipitate. The solution was extracted with ether-hexane (1:1) (1×4 L, 3×2 L). 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 (300 MHz, CDCl3): 0.30 (s 9H), 2.34 (s, 3H), 7.19 (d, 7.7 Hz, 2H), 7.40 (d, 7.7 Hz, 2H).

Aufarbeitung

  1. temperaturemaintaining the temperature below -5° C.
  2. dissolutionto dissolve the precipitate
  3. extractionThe solution was extracted with ether-hexane (1:1) (1×4 L, 3×2 L)
  4. washThe combined organic phases were washed with brine
  5. dry with materialdried over magnesium sulfate
  6. customthe solvents removed under vacuum
  7. customPurification by flash chromatography on silica gel
  8. washeluting with hexane/ethyl acetate (95:5)
  9. customgave a pale yellow oil
  10. customwere removed by filtration

Quellen und Nachweise

ORD-Eintrag
ord-74a262af77854c29a7b53518fb9b4d76
Quelldatensatz
uspto-grants-1996_12
Patentnummer
US05583130

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