HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Trifluoromethylsulfonyloxy)prop-1-yne → HCID 13931230, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Trifluoromethylsulfonyloxy)prop-1-yne | HCID 3084814 | — |
| Reactant | 1,3-Benzotellurazole | HCID 13214795 | — |
| Reactant | 2-Methyl-1,3-benzotellurazole | HCID 13214796 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13931230 | HCID 13931230 | — |
Reaction Steps
2-Methylbenzotellurazole (Example 18) (0.81 g, 0.0033 mole) was dissolved in dichloromethane (30 ml). A solution in carbon tetrachloride (25 ml) of 2-propyn-1-yl trifluoromethanesulfonate, prepared as described above, (0.004 mole) was placed in a dropping funnel and added at room temperature under a nitrogen atmosphere to the benzotellurazole solution. The mixture was stirred for about 20 hours after the addition was complete, forming a white solid, which was isolated by filtration, washed with dichloromethane, and dried at room temperature under vacuum. Yield 0.60 g (42% of theory), m.p. 150°-152° C. The infrared, nuclear magnetic resonance and mass spectra were consistent with the structural formula.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04661438 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-b738d99c44ad40339aa7afac499da834 |
| Source note | uspto-grants-1987_04 |