HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1617983Generated: November 2, 2026
Trifluoroacetic anhydride → HCID 136167040, compound
https://huagongshe.com/reaction/1617983
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178424250 | HCID 178424250 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 136167040 | HCID 136167040 | 14% |
Reaction Steps
Trifluoroacetic anhydride (421 mg, 2.01 mmol) was added at 0° C. to a suspension of (R,E)-4-(3-(4-(4-carboxypiperidin-1-yl)phenyl)-1-(hydroxyimino)-3-o-tolylpropyl)-2-methyl-pyridine 1-oxide (95 mg, 201 μmol) in dichloromethane (3 mL) to give a white suspension, then after 1 h another portion of trifluoroacetic anhydride (421 mg, 2.01 mmol) was added. The reaction mixture was allowed to reach room temperature over 1 h, then treated with 1 M aq. sodium hydroxide solution and stirred for another 90 min. After extraction with dichloromethane, the organic layer was washed with brine, dried over sodium sulfate, filtered, and evaporated. The residue was purified by preparative HPLC to produce the title compound (13 mg, 14%). Light yellow oil, MS (ESI+): m/z=474.4 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765730B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-3d7a8a285b9c451eb61eed43b735093c |
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| Source note | uspto-grants-2014_07 |
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