Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1991554Generated: November 2, 2026

Pyridine → HCID 60206954, compound

https://huagongshe.com/reaction/1991554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantHCID 68541012HCID 68541012—
SolventEthyl AcetateHCID 8857—
ProductHCID 60206954HCID 6020695450%

Reaction Steps

At 0° C., to a stirred solution of the hydroxy-isobutylbenzamide (3.72 g, 19.3 mmol) in pyridine (15 mL) under argon was added trifluoromethanesulfonic anhydride (10.2 ml, 57.8 mmol). The reaction mixture was eventually warmed up to room temperature and stirred overnight. The reaction was diluted with ethyl acetate, and washed with 1N HCl (×2), water (×1) and brine (×1), dried with sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified by flash column chromatography (5% ethyl acetate: hexane) to afford 2.66 g of the desired product as a clear oil (50% yield). 1H NMR (CDCl3) δ 7.56 (s, 1H), 7.50 (d, J=8 Hz, 1H), 7.43 (d, J=8 Hz, 1H), 2.57 (d, J=8 Hz, 2H), 1.92 (m, 1H), 0.97 (d, J=4 Hz, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645780B2
Source datasetuspto-grants-2010_01
ORD IDord-65922e4b326a45a0822632232257df72
Source noteuspto-grants-2010_01