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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394635Generated: October 27, 2026

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

https://huagongshe.com/reaction/394635

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-dioxa-dibenzo[a,d]cyclooctene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06602901B2
Source datasetuspto-grants-2003_08
ORD IDord-174b2d4714da47b4ba1fe96d04b8e68f
Source noteuspto-grants-2003_08