HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitric Acid → 2-nitro-S-(trifluoromethyl)dibenzothiophenium trifluoromethanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | 5-(Trifluoromethyl)dibenzothiophenium trifluoromethanesulfonate | HCID 2777507 | — |
| Reactant | Nitronium Trifluoromethanesulfonate | HCID 10878049 | — |
| Solvent | Nitromethane | HCID 6375 | — |
| Product | 2-nitro-S-(trifluoromethyl)dibenzothiophenium trifluoromethanesulfonate | HCID 86745227 | 76% |
Reaction Steps
A mixture of 0.058 ml (1.3 mmol) of 94% nitric acid and 0.266 ml (1.58 mmol) of trifluoromethanesulfonic anhydride was stirred at room temperature for 1.5 hours to prepare nitronium trifluoromethanesulfonate, and then 2 ml of nitromethane and 502 mg (1 mmol) of S-(trifluoromethyl)dibenzothiophenium trifluoromethanesulfonate was added to the mixture. The reaction mixture was stirred overnight at room temperature and concentrated under reduced pressure. Diethyl ether was added to the residue and the resulting precipitate was collected by filtration to give 339 mg (76%) of 2-nitro-S-(trifluoromethyl)dibenzothiophenium trifluoromethanesulfonate as pale yellow crystals. The properties of the product are summarized in Table 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05066795 |
| Source dataset | uspto-grants-1991_11 |
| ORD ID | ord-580f061aba05415f9600b14a33a645d4 |
| Source note | uspto-grants-1991_11 |