HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593361Generated: October 31, 2026
Hydrogen Peroxide → 3-Chloro-6,7-dihydro-5h-cyclopenta[b]pyridine 1-oxide
https://huagongshe.com/reaction/593361
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | 3-Chloro-6,7-dihydro-5H-cyclopenta[b]pyridine | HCID 68107814 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-Chloro-6,7-dihydro-5h-cyclopenta[b]pyridine 1-oxide | HCID 58082839 | — |
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 sulphate 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%). (calculated) C8H8ClNO [169.61]; (found) [M+H]+=170.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242943B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-e49ee86c8e324c05a138f0f4379ee78f |
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| Source note | uspto-grants-2016_01 |
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