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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067863Generated: November 1, 2026

N-bromobutanimide → 12-bromo-2,10-dichloro-12H-5,7-dioxadibenzo[a,d]cyclooctene

https://huagongshe.com/reaction/1067863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2,10-dichloro-12H-dibenzo[d,g][1,3]dioxocineHCID 14900556—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
Product12-bromo-2,10-dichloro-12H-5,7-dioxadibenzo[a,d]cycloocteneHCID 2272777827%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 2,10-dichloro-12H-dibenzo[d,g][1,3]-dioxocin (21.4 g, 76.1 mmol) and N-bromosuccinimide (13.5 g, 76.1 mmol) in tetrachloromethane (275 mL) was added azobisisobutyronitrile (200 mg, 1.2 mmol). The mixture was heated at 80° C. for 24 h. Another 3×azobisisobutyronitrile (200 mg, 1.2 mmol) was added within the 24 h. The mixture was filtrated and the solution phase concentrated in vacuo. The residue was added dichloromethane (30 mL) and ether (100 mL). The mixture was filtered and the solution phase concentrated in vacuo. The residue was submitted to flash chromatography eluting with heptane/ethyl acetate (3:1) to give 7.4 g (27%) of 12-bromo-2,10-dichloro-12H-5,7-dioxadibenzo[a,d]cyclooctene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248781B1
Source datasetuspto-grants-2001_06
ORD IDord-67236d7dc3714696b34a751a5fd20d3e
Source noteuspto-grants-2001_06