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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium DithioniteHCID 24489—
Reactant2,4-Dibromo-6-methyl-3-nitropyridineHCID 10402274—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2,4-Dibromo-6-methylpyridin-3-amineHCID 1008423899%

Reaction Conditions

Temperature65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176306B2
Source datasetuspto-grants-2007_02
ORD IDord-4131832e4d8043c3a11f9c32fdd844e3
Source noteuspto-grants-2007_02