HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598403Generated: October 29, 2026
tert-Butyl hydroperoxide → 4-Chloro-5-nitropyridin-2(1H)-one
https://huagongshe.com/reaction/598403
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl hydroperoxide | HCID 6410 | — |
| Reactant | 4-Chloro-3-nitropyridine | HCID 2735781 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Chloro-5-nitropyridin-2(1H)-one | HCID 42609067 | 35% |
Reaction Steps
Anhydrous THF (50 mL) in a 500-mL round-bottom flask was cooled to −78° C. and anhydrous NH3 (gas) was bubbled into until saturated (about 20 minutes). Potassium t-butoxide (6.5 g, 57.9 mmol) was added portion wise and the mixture was allowed to warm to ˜35° C. To a solution of 4-chloro-3-nitropyridine (3.498 g, 22 mmol) in dry THF (20 mL) at 0° C. was added tBOOH (4.4 mL, 22 mmol) (5M in decane) over 10 minutes. This solution was then added dropwise to the prepared KOtBu solution over a period of 15 minutes, then stirred for 2 hours at ˜35° C., followed by quenching the reaction with 5 mL of saturated aqueous NH4Cl solution. The reaction was allowed to stir at room temperature overnight. Volatiles were removed under reduced pressure and the residue was made weakly acidic with saturated aqueous NH4Cl solution. The solid was filtered and washed with cold water. The title compound was obtained as a tan-powder, dried under high vacuum overnight, and used for the next reaction without further purification. (1.36 g, 35% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897624B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-9cc4954a1449421997bdbb59a935cbf3 |
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| Source note | uspto-grants-2011_03 |
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