HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427263Generated: October 31, 2026
Azobisisobutyronitrile → 2-(Bromomethyl)-6-fluoropyridine
https://huagongshe.com/reaction/2427263
Participants
| Role | Name | HCID | Charge |
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| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Fluoro-6-methylpyridine | HCID 96090 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(Bromomethyl)-6-fluoropyridine | HCID 13985218 | — |
Reaction Steps
Add NBS (35.6 g, 0.20 mole) to a solution of 6-fluoro-2-methylpyridine (20 mL, 0.19 mole) in EtOAc (400 mL) at room temperature. When the temperature reaches 45° C., add AIBN (400 mg, 2.4 mmol). Heat the mixture at 65° C. for 6 h, then cool to room temperature and add hexane (1 L). Remove the white precipitate by filtration and wash the solid with hexane/EtOAc (1:1). Wash the filtrate with small amounts of aqueous Na2S2O3, NaHCO3, and brine. Dry the organics (Na2SO4), filter, then remove most of the solvent under vacuum at room temperature. Transfer the remaining solution to a distillation set-up. Remove the remaining solvent by distilling at atmospheric pressure, followed by the unreacted starting material at 80 mm (bp ca 70° C.; 11.2 g) and then the title product at 1 mm (bp ca 75° C.; 12.1 g, 32%). NMR (300 MHz; CDCl3): 7.82 (1H; dd); 7.35 (1H; dd); 6.90 (1H; dd); 4.50 (2H; s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07968587B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-965146ba5115477bbbd329ced55b5460 |
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| Source note | uspto-grants-2011_06 |
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