Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | Propanediol | HCID 134919 | — |
| Reactant | HCID 86620802 | HCID 86620802 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178505439 | HCID 178505439 | — |
Reaction Steps
Propanediol (0.3 mole) is cooled under a nitrogen atmosphere to a temperature of 0° C. Then 4-bromo-3,5-difluorophenylbenzoylchloride (0.3 mole) are swiftly added with continuous stirring. The reaction mixture is then cooled to −10° C. and triflic acid (0.45 mole) is added. The reaction mixture is stirred further for 1 hour, then acetic anhydride (2 mole) is added maintaining the temperature below 5° C. After adding diethyl ether and stirring for 1 more hour at −10° C., 4-bromo-3,5-difluorophenyl-thianylium triflate is filtered off and washed with cold ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07544400B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-4e2485d129184009bda3326929f6051a |
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| Source note | uspto-grants-2009_06 |
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