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HRID 543093作成日:2026年10月26日
Ethyl (((trifluoromethyl)sulfonyl)oxy)acetate → 3-Ethoxycarbonylmethyl-2-methylbenzotellurazolium Trifluoromethanesulfonate
https://huagongshe.com/reaction/543093
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl (((trifluoromethyl)sulfonyl)oxy)acetate | HCID 371745 | — |
| 反応物 | 1,3-Benzotellurazole | HCID 13214795 | — |
| 反応物 | 2-Methyl-1,3-benzotellurazole | HCID 13214796 | — |
| 溶媒 | Carbon Tetrachloride | HCID 5943 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 3-Ethoxycarbonylmethyl-2-methylbenzotellurazolium Trifluoromethanesulfonate | HCID 13931234 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04661438 |
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| 出典データセット | uspto-grants-1987_04 |
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| ORD ID | ord-85d05d9e9e2b4624968622006817a472 |
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| 出典メモ | uspto-grants-1987_04 |
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