HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505383Generated: October 26, 2026
Hydrochloric Acid → 2-Chloro-3-methyl-1-oxo-1lambda~5~-pyridine
https://huagongshe.com/reaction/505383
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Urea | HCID 1176 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | Carbamide Peroxide | HCID 31294 | — |
| Reactant | 2-Chloro-3-methylpyridine | HCID 87603 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-3-methyl-1-oxo-1lambda~5~-pyridine | HCID 13431622 | 63% |
Reaction Steps
Into a mixture of 2-chloro-3-methylpyridine (12.8 g, 100 mmol), urea hydrogen peroxide addition compound ((NH2)2CO.H2O2, 19.8 g, 210 mmol) and dichloromethane (130 ml) was added dropwise anhydrous trifluoroacetic acid (28.2 ml, 200 mmol) at 0° C. under nitrogen flow, and the reaction mixture was stirred at 0° C. for 1 hour. Then, after stirring for 30 minutes and elevating the reaction temperature to room temperature, an aqueous solution (200 ml) of sodium hydrosulfite (20 g) was added, and the reaction mixture was stirred for 15 minutes. 2N hydrochloric acid (50 ml) was added and the mixture was extracted with dichloromethane (120 ml), and after washed with sodium bicarbonate solution, the mixture was dried over magnesium sulfate and the solvent was evaporated, thereby yielding the title compound (9.00 g, 62.7 mmol, 63%) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07781452B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-ed9b942820084dbeb4e4a32f7027b488 |
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| Source note | uspto-grants-2010_08 |
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