Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121714Generated: November 3, 2026

N-bromobutanimide → 3-(Bromomethyl)-2,5-dichlorothiophene

https://huagongshe.com/reaction/2121714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2,5-Dichloro-3-methylthiopheneHCID 268910—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
Product3-(Bromomethyl)-2,5-dichlorothiopheneHCID 2343408291.1%

Reaction Steps

To a stirred solution of 2,5-dichloro-3-methylthiophene (25.8 g, 154 mmol) in carbon tetrachloride (47 mL) was added N-bromosuccinimide (27.5 g, 154 mmol) and benzoyl peroxide (310 mg, 1.28 mmol). The mixture was heated at reflux temperature for 8 hours. After cooling, the insolubles were filtered off. The filtrate was washed with aqueous sodium sulfite solution, dried over MgSO4, and concentrated in vacuo. The residue was fractionally distilled under reduced pressure (bp 80° C., 0.5 mmHg) to give the subtitle compound (34.5 g, 91% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696470B2
Source datasetuspto-grants-2004_02
ORD IDord-1af66f65e8ce4500976f36b61b2ee0ae
Source noteuspto-grants-2004_02