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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075562Generated: October 31, 2026

N-bromobutanimide → HCID 58370234, compound

https://huagongshe.com/reaction/2075562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-(Methanesulfonyl)-5-methylpyridineHCID 23437039—
ReactantHCID 58370163HCID 58370163—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 58370234HCID 58370234—

Reaction Steps

To a solution of 0.25 g of 2-methanesulfonyl-5-methyl-pyridine (from the preparation of 5-bromomethyl-2-methanesulfinyl-pyridine, step b)) in 20 mL carbon tetrachloride was added 0.27 g NBS and 4 mg benzoyl peroxide. This mixture was refluxed for 4 hours. The reaction mixture was cooled to room temperature, washed with aqueous sodium hydrogen carbonate solution, dried over sodium sulphate, and concentrated to dryness. Purification by flash chromatography (silica, heptane/ethyl acetate) provided 0.11 g of 5-bromomethyl-2-methanesulfonyl-pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919628B2
Source datasetuspto-grants-2011_04
ORD IDord-7d613228cb4246c792ef02193f3ee4e6
Source noteuspto-grants-2011_04