HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dibenzofuran → 1-Bromodibenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dibenzofuran | HCID 568 | — |
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Bromodibenzofuran | HCID 190542 | — |
Reaction Steps
Under nitrogen current at −78° C., an n-butyl lithium hexane solution (1.6M, 69 ml) is dropped to a THF solution (175 ml) containing 16.82 g of dibenzofuran, and the temperature of the mixture is raised to room temperature over 80 minutes. The obtained solution is again cooled to −78° C., 19.0 ml of 1,2-dibromoethane is added to the solution, and the temperature of the solution is raised to room temperature over 120 minutes. Water is added to the obtained reaction solution to stop the reaction. Organic layers extracted from the obtained mixture with ethyl acetate are dried with sodium sulfate, and then concentrated with an evaporator to obtain 12.35 g of Compound 16-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08211551B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-1475262ba7e045a3a7e2a397513bdafa |
| Source note | uspto-grants-2012_07 |