HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 622849Erstellt: 26. Oktober 2026
Benzyl trifluoromethanesulfonate → 3-Benzyl-2-methylbenzotellurazolium Trifluoromethanesulfonate
https://huagongshe.com/reaction/622849
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Benzyl trifluoromethanesulfonate | HCID 11096711 | — |
| Edukt | 1,3-Benzotellurazole | HCID 13214795 | — |
| Edukt | 2-Methyl-1,3-benzotellurazole | HCID 13214796 | — |
| Lösungsmittel | Carbon Tetrachloride | HCID 5943 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 3-Benzyl-2-methylbenzotellurazolium Trifluoromethanesulfonate | HCID 13931232 | — |
Reaktionsschritte
2-Methylbenzotellurazole (Example 18) (0.81 g), 0.0033 mole) was dissolved in dichloromethane (25 ml). The solution of benzyl trifluoromethanesulfonate (0.004 mole) in carbon tetrachloride, prepared as described above, was placed in a dropping funnel and added at room temperature under a nitrogen atmosphere to the benzotellurazole solution. Stirring was continued for 18 hours at room temperature after the addition was complete, maintaining a nitrogen atmosphere. The solid was isolated by filtration, washed with diethyl ether, and dried at room temperature under a vacuum. Yield 0.30 g (19% of theory) of a white powder, m.p. 120°-122° C. The infrared, nuclear magnetic resonance, and mass spectra of this compound were in agreement with that expected for the structural formula.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04772715 |
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| Quelldatensatz | uspto-grants-1988_09 |
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| ORD ID | ord-e4b5cf6ddcd344cd8f23044260c3f17e |
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| Quellennotiz | uspto-grants-1988_09 |
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