Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497476Generated: October 27, 2026

Isopropyl iodide → HCID 59541857, compound

https://huagongshe.com/reaction/1497476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Hydroxy-5-iodopyridineHCID 459500—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 59541857HCID 5954185786.6%

Reaction Steps

To a stirred solution 5-iodopyridin-2-ol (0.4 g, 1.80 mmol) in DME (10 mL) was added t-BuOK (0.604 g, 5.4 mmol). The mixture was stirred for 30 min at rt, K2CO3 (0.621 g, 4.5 mmol) and 2-iodopropane (0.35 mL, 3.6 mmol) were added, and the reaction was heated at reflux for about 3 h. The reaction mixture was diluted with water (30 mL) and extracted with ethyl acetate (2×100 mL). The combined organic extracts were washed with brine solution (10 mL), dried over Na2SO4 and concentrated under vacuum to obtain crude product. The crude product was purified by flash chromatography (silica gel, 60-120μ) using 10% ethyl acetate in hexane as eluent to afford 5-iodo-1-isopropylpyridin-2(1H)-one as an off-white solid (0.41 g, 67% yield). 1H NMR (400 MHz, DMSO-d6): δ 7.90 (s, 1H), 7.49 (dd, 1H), 6.21 (d, 1H), 4.94 (t, 1H), 1.25 (t, 6H), LC-MS m/z calcd for [M+H]+ 263.98. found 264.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199975B2
Source datasetuspto-grants-2015_12
ORD IDord-5ad7a70690c748e29e4d321d88b40280
Source noteuspto-grants-2015_12