Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 622847생성일: 2026년 10월 25일
Ethyl (((trifluoromethyl)sulfonyl)oxy)acetate → 3-Ethoxycarbonylmethyl-2-methylbenzotellurazolium Trifluoromethanesulfonate
https://huagongshe.com/reaction/622847
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl (((trifluoromethyl)sulfonyl)oxy)acetate | HCID 371745 | — |
| 반응물 | 1,3-Benzotellurazole | HCID 13214795 | — |
| 반응물 | 2-Methyl-1,3-benzotellurazole | HCID 13214796 | — |
| 용매 | Carbon Tetrachloride | HCID 5943 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 3-Ethoxycarbonylmethyl-2-methylbenzotellurazolium Trifluoromethanesulfonate | HCID 13931234 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04772715 |
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| 출처 데이터셋 | uspto-grants-1988_09 |
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| ORD ID | ord-3abd1d49cfd44e4a86ffad7063528594 |
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| 출처 메모 | uspto-grants-1988_09 |
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