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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

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl (((trifluoromethyl)sulfonyl)oxy)acetateHCID 371745—
反応物1,3-BenzotellurazoleHCID 13214795—
反応物2-Methyl-1,3-benzotellurazoleHCID 13214796—
溶媒Carbon TetrachlorideHCID 5943—
溶媒DichloromethaneHCID 6344—
生成物3-Ethoxycarbonylmethyl-2-methylbenzotellurazolium TrifluoromethanesulfonateHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04661438
出典データセットuspto-grants-1987_04
ORD IDord-85d05d9e9e2b4624968622006817a472
出典メモuspto-grants-1987_04