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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555413Generated: October 25, 2026

Water → HCID 178440819, compound

https://huagongshe.com/reaction/555413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium IodideHCID 5238—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantAluminumHCID 5359268—
Reactant2-(2-tert-Butyl-phenoxy)-6-methoxy-3-nitro-pyridineHCID 59857403—
SolventPyridineHCID 1049—
SolventAcetonitrileHCID 6342—
ProductHCID 178440819HCID 17844081958%

Reaction Steps

Sodium iodide (10.6 g, 71 mmol) was added to a green solution of 2a (4.26 g, 14 mmol) in acetonitrile (80 mL) in a vessel covered with aluminum foil to protect from light, followed by chlorotrimethylsilane (8.9 mL, 71 mmol) and water (0.4 mL, 21 mmol). The yellow-orange mixture was refluxed overnight in the dark. HPLC analysis showed that although some starting pyridine was still present, decomposition also appeared to be occurring. The reaction was quenched with saturated sodium thiosulfate solution (30 mL). The resulting mixture was extracted with ethyl acetate (3×50 mL). The combined organic layer was washed with brine (30 mL), dried over sodium sulfate, and concentrated to give a yellow oil. The oil was purified by SiO2 chromatography (120 g), loaded with CH2Cl2 and eluted using a gradient of ethyl acetate in hexanes to afford 136a (2.34 g, 58% yield) as a yellow waxy solid, HPLC purity 100%, 3.66 min (Method A); [M+H]+=289.17; in 1H NMR (500 MHz, CDCl3) δ ppm 8.42 (d, 1H, J=5.0 Hz), 7.48 (m, 1H), 7.18 (m, 2H), 6.92 (m, 1H), 6.33 (d, 1H, J=10.0 Hz), 1.37 (s, 9H); 13C (125 MHz, CDCl3) δ (ppm), 163.87, 155.70, 150.61, 142.05, 139.87, 127.86, 126.83, 125.98, 122.98, 104.62, 34.68, 30.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053450B2
Source datasetuspto-grants-2011_11
ORD IDord-1b2bb6d9ea8646f897881ef3a0ffe95b
Source noteuspto-grants-2011_11