HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446708Generated: October 28, 2026
Azobisisobutyronitrile → HCID 68541623, compound
https://huagongshe.com/reaction/1446708
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Iodo-2-methylpyridine | HCID 12691322 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 68541623 | HCID 68541623 | — |
Reaction Steps
Combine 4-iodo-2-methyl-pyridine (1.1 g, 5 mmol), NBS (0.98 g, 1.1 equiv.) and carbon tetrachloride (50 mL) in a round bottomed flask under nitrogen. Add AIBN (82 mg, 0.1 equiv.) and heat reaction overnight at reflux. Filter the reaction, washing with hexanes. Concentrate filtrate to approximately 10-20 mL volume. Redissolve in THF (20 mL) and cool to 0° C. under nitrogen. Add diethylamine (1.04 mL, 2 equiv.) dropwise via syringe and stir one hour at 0° C. Remove cooling bath and let warm to room temperature. After 6 hours total, concentrate to dryness and purify by silica gel (1:1 Hexanes:Ethyl Acetate→Ethyl Acetate) to give a tan liquid (0.51 g, 35% over 2 steps). MS (ES), m/z 291.0 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07666879B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-ce69ba0adb55448cb7d409c49c272306 |
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| Source note | uspto-grants-2010_02 |
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