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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440656Generated: October 29, 2026

N-bromobutanimide → 3-Bromo-4-chloro-2,3-dihydro-2,2-dimethyl-7-nitrobenzofuran

https://huagongshe.com/reaction/440656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant4-Chloro-2,3-dihydro-2,2-dimethyl-7-nitrobenzofuranHCID 22404776—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
Product3-Bromo-4-chloro-2,3-dihydro-2,2-dimethyl-7-nitrobenzofuranHCID 2240481595.4%

Reaction Steps

A mixture of 11.82 g (0.052 mole) of 4-chloro-2,3-dihydro-2,2-dimethyl-7-nitrobenzofuran (Example 1, Step C) and 9.3 g (0.052 mole) of N-bromosuccinimide in 200 mL of carbon tetrachloride was irradiated with a sun lamp for approximately 16 hours. No reaction occurred during this time. To this mixture was then added 0.10 g of benzoyl peroxide, and the reaction mixture was then heated at reflux and irradiated simultaneously for a period of five hours. The sun lamp was turned off, and the mixture was allowed to stir while being heated at reflux for an additional hour. The mixture was then passed through a column of silica gel, and product-containing fractions were combined. The solvent was evaporated from the combined fractions under reduced pressure, leaving 15.2 g of 3-bromo-4-chloro-2,3-dihydro-2,2-dimethyl-7-nitrobenzofuran as a solid, m.p. 103°-104° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521147
Source datasetuspto-grants-1996_05
ORD IDord-e054de35a3e44bf4a04a6d695b45b00d
Source noteuspto-grants-1996_05