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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl (((trifluoromethyl)sulfonyl)oxy)acetateHCID 371745—
Reactant1,3-BenzotellurazoleHCID 13214795—
Reactant2-Methyl-1,3-benzotellurazoleHCID 13214796—
SolventCarbon TetrachlorideHCID 5943—
SolventDichloromethaneHCID 6344—
Product3-Ethoxycarbonylmethyl-2-methylbenzotellurazolium TrifluoromethanesulfonateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04661438
Source datasetuspto-grants-1987_04
ORD IDord-85d05d9e9e2b4624968622006817a472
Source noteuspto-grants-1987_04