HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 6-Bromo-1-benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Bromo-3-(2,2-diethoxyethoxy)benzene | HCID 15453765 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6-Bromo-1-benzofuran | HCID 15158722 | 72.9% |
Reaction Steps
To a solution of 1-bromo-3-(2,2-diethoxyethoxy)benzene (2.3 g, 8.35 mmol) in toluene (28 mL), was added PPA (5.0 mL) and refluxed for overnight. The reaction solution was added water at room temperature, and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, concentrated in vacuo, and purified by silica-gel column chromatography (hexane). The title compound (1.2 g (yield 68%, mixture with 7-bromobenzofuran)) was obtained as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08551985B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-23f29aeb25d443e289ced8877ec25bbe |
| Source note | uspto-grants-2013_10 |