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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1806018Generated: October 31, 2026

Benzoyl Peroxide → 2-(1-Bromoethyl)pyridine

https://huagongshe.com/reaction/1806018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
Reactant2-EthylpyridineHCID 7523—
ReactantN-bromobutanimideHCID 67184—
SolventCarbon TetrachlorideHCID 5943—
Product2-(1-Bromoethyl)pyridineHCID 1537365749.9%

Reaction Steps

2-Ethylpyridine (20.0 g, 186.65 mmol) was placed in carbon tetrachloride (830 mL) and benzoyl peroxide (4.5211 g, 18.665 mmol) and 1-bromopyrrolidine-2,5-dione (33.221 g, 186.65 mmol) were added. The reaction mixture was heated to reflux for 18 hours, then cooled to room temperature and filtered. The filtrate was concentrated and the residue was purified over a plug of silica to give 2-(1-bromoethyl)pyridine (17.312 g, 49.9%). 1H NMR (CDCl3) δ 8.58 (d, 1H), 7.69 (td, 1H), 7.76 (d, 1H), 7.20 (dd, 1H), 5.24 (q, 1H), 2.08 (d, 3H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354540B2
Source datasetuspto-grants-2013_01
ORD IDord-b9febb3c3fa249a2a11c2718815040a8
Source noteuspto-grants-2013_01