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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508994Generated: October 31, 2026

Isopropanol → 4-chloro-2-isopropoxy-6,7-dihydro-5H-cyclopenta[b]pyridine oxide

https://huagongshe.com/reaction/1508994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant2,4-Dichloro-6,7-dihydro-5H-cyclopenta[b]pyridine 1-oxideHCID 90112536—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
Product4-chloro-2-isopropoxy-6,7-dihydro-5H-cyclopenta[b]pyridine oxideHCID 9011077289%

Reaction Steps

To a solution of iso-propanol (0.047 g, 0.79 mmol) in dioxane (3 mL) at rt was added potassium tert-butoxide (0.053 g, 0.47 mmol). The mixture was stirred at rt for 30 min. Then, 2,4-dichloro-6,7-dihydro-5H-cyclopenta[b]pyridine 1-oxide (0.100 g, 0.39 mmol) in dioxane (1 mL) was added and the mixture was heated under microwave irradiation to 100° C. for 30 min. After this time, the mixture was diluted with methylene chloride and washed with water. The organic layer were dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated. The residue was purified by column chromatography (silica, dichloromethane/methanol) to afford the title compound (0.079 g, 88%) as a white solid. MW=227.69. 1H NMR (CDCl3, 300 MHz) δ 6.73 (s, 1H), 4.90-4.85 (m, 1H), 3.23 (t, J=7.5 Hz, 2H), 3.00 (t, J=7.5 Hz, 2H), 2.20 (quin, J=7.5 Hz, 2H), 1.44 (d, J=6.0 Hz, 6H); APCI MS m/z 228 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221843B2
Source datasetuspto-grants-2015_12
ORD IDord-26239ae189e14d3eb86160e925eadca7
Source noteuspto-grants-2015_12