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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004168Generated: November 2, 2026

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

https://huagongshe.com/reaction/1004168

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 numberUS06048880
Source datasetuspto-grants-2000_04
ORD IDord-0bdfe2261e10431a8fe862dfc87a5c9b
Source noteuspto-grants-2000_04