Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | HCID 19737928 | HCID 19737928 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,3-dibromo-dibenzofuran | HCID 526288 | 116.4% |
Reaction Steps
To a solution of t-butylnitrite (0.89 ml, 7.2 mmol) dissolved in 10 ml of DMF at 50° C. was added dropwise a solution of 2-amino-1,3-dibromodibenzofuran 17 (1.0 g, 2.9 mmol) in 10 ml of DMF with nitrogen evolution. After stirring at 50° C. for 1 hour the reaction was diluted into ether and washed successively with H2O and saturated NaCl. Drying over MgSO4 and evaporation gave 1.1 g of a red solid which was purified by flash chromatography through 100 g of silica gel (20% methylene chloride: hexane) yielding 650 mg (68%) of the title compound as a pale orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05132420 |
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| Source dataset | uspto-grants-1992_07 |
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| ORD ID | ord-5e8e6bc24bba4ec0b15bdcda33695775 |
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| Source note | uspto-grants-1992_07 |
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