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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296141Generated: November 1, 2026

Pyridine → HCID 60206954, compound

https://huagongshe.com/reaction/1296141

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 numberUS07244725B2
Source datasetuspto-grants-2007_07
ORD IDord-203ae74233ac4986b4ddb6bae53f5851
Source noteuspto-grants-2007_07