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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2,3-Dichloro-6-methylpyridineHCID 15271418—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
Product6-(Bromomethyl)-2,3-dichloropyridineHCID 8979347897.9%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328096B2
Source datasetuspto-grants-2016_05
ORD IDord-63d69bc5bb9c4944841db91c4f54a566
Source noteuspto-grants-2016_05