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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543095Generated: October 26, 2026

Benzyl trifluoromethanesulfonate → 3-Benzyl-2-methylbenzotellurazolium Trifluoromethanesulfonate

https://huagongshe.com/reaction/543095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl trifluoromethanesulfonateHCID 11096711—
Reactant1,3-BenzotellurazoleHCID 13214795—
Reactant2-Methyl-1,3-benzotellurazoleHCID 13214796—
SolventCarbon TetrachlorideHCID 5943—
SolventDichloromethaneHCID 6344—
Product3-Benzyl-2-methylbenzotellurazolium TrifluoromethanesulfonateHCID 13931232—

Reaction Steps

2-Methylbenzotellurazole (Example 18) (0.81 g, 0.0033 mole) was dissolved in dichloromethane (25 ml). The solution of benzyl trifluoromethanesulfonate (0.004 mole) in carbon tetrachloride, prepared as described above, was placed in a dropped funnel and added at room temperature under a nitrogen atmosphere to the benzotellurazole solution. Stirring was continued for 18 hours at room temperature after the addition was complete, maintaining a nitrogen atmosphere. The solid was isolated by filtration, washed with diethyl ether, and dried at room temperature under a vacuum. Yield 0.30 g (19% of theory) of a white powder, m.p. 120°-122° C. The infrared, nuclear magnetic resonance, and mass spectra of this compound were 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-86c063819a924bb49e18de25413ecdb8
Source noteuspto-grants-1987_04