HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → Benzyl trifluoromethanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | 2-Propen-1-yl 1,1,1-trifluoromethanesulfonate | HCID 10932223 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Benzyl trifluoromethanesulfonate | HCID 11096711 | — |
Reaction Steps
Benzyl trifluoromethanesulfonate was prepared in carbon tetrachloride solution and used as a dried solution in Examples 52 through 54, in the same way the 2-propen-1-yl trifluoromethanesulfonate was prepared and used in Examples 40 through 43, starting with benzyl alcohol and trifluoromethanesulfonic anhydride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04772715 |
| Source dataset | uspto-grants-1988_09 |
| ORD ID | ord-306710b1eb794776a8c9a2e30ecea575 |
| Source note | uspto-grants-1988_09 |