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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

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl (((trifluoromethyl)sulfonyl)oxy)acetateHCID 371745—
반응물1,3-BenzotellurazoleHCID 13214795—
반응물2-Methyl-1,3-benzotellurazoleHCID 13214796—
용매Carbon TetrachlorideHCID 5943—
용매DichloromethaneHCID 6344—
생성물3-Ethoxycarbonylmethyl-2-methylbenzotellurazolium TrifluoromethanesulfonateHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04772715
출처 데이터셋uspto-grants-1988_09
ORD IDord-3abd1d49cfd44e4a86ffad7063528594
출처 메모uspto-grants-1988_09