HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522159Generated: October 28, 2026
N-bromobutanimide → 6-(Bromomethyl)-2,3-dichloropyridine
https://huagongshe.com/reaction/522159
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2,3-Dichloro-6-methylpyridine | HCID 15271418 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 6-(Bromomethyl)-2,3-dichloropyridine | HCID 89793478 | 97.9% |
Reaction Steps
To a solution of 2,3-dichloro-6-methylpyridine (2 g, 12.3 mmol) in carbon tetrachloride (40 mL) was added NBS (2.64 g, 14.8 mmol) followed by AIBN (40 mg, 0.24 mmol). The reaction heated to 80° C. under nitrogen for 3.5 hours. The reaction was cooled and concentrated in vacuo. The residue was sonicated in heptanes and filtered. The filtrate was eluted through a pad of silica using 10% TBME in heptanes to afford the title compound (2.90 g). The crude material was taken on directly to the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09328096B2 |
|---|
| Source dataset | uspto-grants-2016_05 |
|---|
| ORD ID | ord-63d69bc5bb9c4944841db91c4f54a566 |
|---|
| Source note | uspto-grants-2016_05 |
|---|