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
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2,10-dichloro-12H-dibenzo[d,g][1,3]dioxocine | HCID 14900556 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 12-bromo-2,10-dichloro-12H-5,7-dioxadibenzo[a,d]cyclooctene | HCID 22727778 | 27% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06602901B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-174b2d4714da47b4ba1fe96d04b8e68f |
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| Source note | uspto-grants-2003_08 |
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