HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361815Generated: October 28, 2026
2,6-Dibromopyridine → HCID 23144486, compound
https://huagongshe.com/reaction/1361815
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Dibromopyridine | HCID 12274 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 23144082 | HCID 23144082 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23144486 | HCID 23144486 | 31% |
Reaction Steps
A THF solution (10 mL) of 2,6-dibromopyridine (4.97 g, 21.0 mmol) was added to a 2.0 mol/L solution of isopropylmagnesium chloride in THF (9.56 mL, 10.1 mmol) at 0° C., followed by stirring for 3 hours at room temperature. A THF solution (5 mL) of Compound 98 (1.37 g, 3.82 mmol) was added dropwise to the reaction mixture, followed by stirring for 3 hours at room temperature. The reaction mixture was poured into a saturated aqueous solution of ammonium chloride, followed by extraction with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate, and then the solvent was distilled away under reduced pressure. The resulting residue was purified through silica gel column chromatography (chloroform:methanol=9:1) to afford the entitled Compound 300 (520 mg, 31%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07880013B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-dc9c5cae161f453d83eb0d4e75bd1166 |
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| Source note | uspto-grants-2011_02 |
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