HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472790Generated: October 31, 2026
Trifluoromethanesulfonic anhydride → Methyl 3-(((trifluoromethyl)sulfonyl)oxy)quinoline-8-carboxylate
https://huagongshe.com/reaction/472790
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methyl 3-hydroxyquinoline-8-carboxylate | HCID 57440941 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 3-(((trifluoromethyl)sulfonyl)oxy)quinoline-8-carboxylate | HCID 58056975 | 91% |
Reaction Steps
Trifluoromethanesulfonic anhydride (0.55 mL, 3.4 mmol) was added to a solution of methyl 3-hydroxyquinoline-8-carboxylate (650 mg, 3.2 mmol) in pyridine (2.3 mL) and CH2Cl2 (13 mL) at 0° C. The reaction mixture was allowed to warm to room temperature. After 3 h, additional trifluoromethanesulfonic anhydride (0.55 mL, 3.4 mmol) was added and the reaction was stirred for an additional 18 h. Saturated aqueous NaHCO3 (20 mL) was added and the layers were separated. The aqueous phase was extracted with CH2Cl2 (3×). The combined organic phase was dried (MgSO4), filtered and concentrated in vacuo. The resulting residue was purified on silica gel eluting with CH2Cl2 to afford 971 mg (91%) of methyl 3-(((trifluoromethyl)sulfonyl)oxy)quinoline-8-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633220B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-4a8e6bba1a38401f95540a4a7f4a9cd5 |
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| Source note | uspto-grants-2014_01 |
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