HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543093Generated: October 25, 2026
Ethyl (((trifluoromethyl)sulfonyl)oxy)acetate → 3-Ethoxycarbonylmethyl-2-methylbenzotellurazolium Trifluoromethanesulfonate
https://huagongshe.com/reaction/543093
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl (((trifluoromethyl)sulfonyl)oxy)acetate | HCID 371745 | — |
| 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-Ethoxycarbonylmethyl-2-methylbenzotellurazolium Trifluoromethanesulfonate | HCID 13931234 | — |
Reaction Steps
2-Methylbenzotellurazole (Example 18) (0.81 g, 0.0033 mole) was dissolved in dichloromethane (30 ml). The solution of ethoxycarbonylmethyl trifluoromethanesulfonate (0.004 mole) in carbon tetrachloride prepared as described above, was placed in a dropping funnel and added to the benzotellurazole solution at room temperature under a nitrogen atmosphere. After the addition was complete, the mixture was stirred at room temperature, while maintaining a nitrogen atmosphere for 22 hours. The solid was isolated by filtration and dried at room temperature under vacuum. Yield was 0.62 g (39% of theory) of a white powder, m.p. 156°-158° C. The C, H, N and S elemental analyses and the infrared, nuclear magnetic resonance, and mass spectra were all 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-85d05d9e9e2b4624968622006817a472 |
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| Source note | uspto-grants-1987_04 |
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