HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918204Generated: November 2, 2026
Chlorosuccinimide → 4,5-Dichloropyridin-2-amine
https://huagongshe.com/reaction/1918204
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | 2-Amino-4-chloropyridine | HCID 581866 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4,5-Dichloropyridin-2-amine | HCID 10773304 | — |
Reaction Steps
4-Chloro-2-aminopyridine (Matrix Scientific, cat. #23809; 1.29 g, 0.01 mol) is dissolved by stirring in 500 ml of ethyl acetate. A thermometer is placed in the solution to monitor temperature. N-Chlorosuccinimide (13.3 g, 0.01 mol) is added in several portions to keep the solution at room temperature. The solution becomes dark in color and is stirred at room temperature overnight. The supernatant is decanted from the dark solids that formed and transferred to a separatory funnel. The organic solution is washed with 500 ml saturated aqueous sodium bisulfite and then 500 ml brine. The organic layer is dried with MgSO4 and concentrated on a rotovap. The dark brown crude product is chromatographed on 500 g of flash silica-gel eluting with CH2Cl2. Concentration of the appropriate fractions on a rotovap gives a light tan solid. The solid is dissolved in EtOAc and decolorized with activated carbon. EtoAc is removed using a rotovap and the resulting solid is suspended in ice-cold CH2Cl2 and filtered to give the product as a white solid. (MP 142-143° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08618302B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-40813e47bb624e378918fcbbd4388d7b |
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| Source note | uspto-grants-2013_12 |
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