HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348555Generated: October 29, 2026
Sodium Dithionite → 2,4-Dibromo-6-methylpyridin-3-amine
https://huagongshe.com/reaction/348555
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | 2,4-Dibromo-6-methyl-3-nitropyridine | HCID 10402274 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,4-Dibromo-6-methylpyridin-3-amine | HCID 10084238 | 99% |
Reaction Steps
2,4-Dibromo-6-methyl-3-nitropyridine (1.0 g, 3.38 mmol) was dissolved in a mixture of methanol (4 mL) and tetrahydrofuran (6 mL), and a solution of sodium hydrosulfite (3.0 g, 17.23 mmol) in water (7 mL) was added thereto over 5 minutes with stirring at 65° C. Subsequently, the mixture was stirred for 30 minutes at 65° C. To the mixture, a solution of sodium hydrosulfite (3.0 g, 17.23 mmol) in water (7 mL) was further added over 5 minutes, and the mixture was stirred for 30 minutes at 65° C. The resultant mixture was allowed to cool, diluted with water, and then the mixture was extracted with chloroform. The organic layer was washed with saturated brine, followed by drying over sodium sulfate anhydrate and concentrating under reduced pressure, to thereby yield 0.89 g of 3-amino-2,4-dibromo-6-methylpyridine as a colorless solid (yield 99%). The product was crystallized from hexane, to thereby obtain colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07176306B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-4131832e4d8043c3a11f9c32fdd844e3 |
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| Source note | uspto-grants-2007_02 |
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