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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1617983Generated: November 2, 2026

Trifluoroacetic anhydride → HCID 136167040, compound

https://huagongshe.com/reaction/1617983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178424250HCID 178424250—
SolventDichloromethaneHCID 6344—
ProductHCID 136167040HCID 13616704014%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765730B2
Source datasetuspto-grants-2014_07
ORD IDord-3d7a8a285b9c451eb61eed43b735093c
Source noteuspto-grants-2014_07