HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543095Generated: October 26, 2026
Benzyl trifluoromethanesulfonate → 3-Benzyl-2-methylbenzotellurazolium Trifluoromethanesulfonate
https://huagongshe.com/reaction/543095
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl trifluoromethanesulfonate | HCID 11096711 | — |
| Reactant | 1,3-Benzotellurazole | HCID 13214795 | — |
| Reactant | 2-Methyl-1,3-benzotellurazole | HCID 13214796 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Benzyl-2-methylbenzotellurazolium Trifluoromethanesulfonate | HCID 13931232 | — |
Reaction Steps
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 dropped 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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04661438 |
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| Source dataset | uspto-grants-1987_04 |
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| ORD ID | ord-86c063819a924bb49e18de25413ecdb8 |
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| Source note | uspto-grants-1987_04 |
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