HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1033412Erstellt: 26. Oktober 2026
Diethyl Ether → Stannane, trimethyl(4-methylphenyl)-
https://huagongshe.com/reaction/1033412
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | Di-p-tolyl | HCID 11941 | — |
| Edukt | Trimethyltin chloride | HCID 14016 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | HCID 178418370 | HCID 178418370 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Stannane, trimethyl(4-methylphenyl)- | HCID 617834 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05310737 |
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| Quelldatensatz | uspto-grants-1994_05 |
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| ORD ID | ord-ae282d93c464437792eb653292e5b568 |
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| Quellennotiz | uspto-grants-1994_05 |
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