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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626128Generated: November 2, 2026

Hydrogen Peroxide → 3-Chloro-6,7-dihydro-5h-cyclopenta[b]pyridine 1-oxide

https://huagongshe.com/reaction/1626128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
Reactant3-Chloro-6,7-dihydro-5H-cyclopenta[b]pyridineHCID 68107814—
SolventAcetic AcidHCID 176—
Product3-Chloro-6,7-dihydro-5h-cyclopenta[b]pyridine 1-oxideHCID 58082839—

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of 3-chloro-6,7-dihydro-5H-[1]pyrindine (3.03 g, 19.7 mmol) in acetic acid (19.7 ml) was treated at room temperature with hydrogen peroxide (3.45 ml, 39.5 mmol). The mixture was heated to 70° C. and stirred at this temperature overnight. After completion, the reaction mixture was allowed to cool and was concentrated at reduced pressure. Water was added and the mixture was evaporated again. This procedure was repeated another 2 times. The residue was dissolved in ethyl acetate, washed with a saturated aqueous solution of sodium hydrogen carbonate and brine, then dried over sodium sulfate and evaporated at reduced pressure. The crude 3-chloro-6,7-dihydro-5H-[1]pyrindine 1-oxide was obtained as dark green crystals (2.07 g, 62% yield). MS (ISP): m/z=170 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785436B2
Source datasetuspto-grants-2014_07
ORD IDord-4561bdeb29454057a1d134c42821bee4
Source noteuspto-grants-2014_07