HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357930Generated: October 30, 2026
N-bromobutanimide → 2,3-Dibromo-6-methoxypyridine
https://huagongshe.com/reaction/2357930
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Bromo-6-methoxypyridine | HCID 256810 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2,3-Dibromo-6-methoxypyridine | HCID 59389317 | — |
Reaction Steps
NBS (302 g) was added to the compound of Example 259 (295 g) in acetonitrile (575 mL) and the mixture was stirred at 80 to 90° C. for 1 day in a nitrogen atmosphere. After cooling, the crystallized imide was removed by filtration and the filtrate was concentrated. Purification of the resulting residue by silica gel column chromatography (ether:petroleum ether=1:1) gave a 6:1 mixture of the title compound and 2,5-dibromo form. This product was crystallized from cold petroleum ether to afford the title compound as a colorless powder (223 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07763617B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-93ee9fdcf12b4cd785e0e92176f5cd17 |
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| Source note | uspto-grants-2010_07 |
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