HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dibromopropane → 3-Phenyl-6-(3-bromopropyloxy)-7-propylbenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Phenyl-7-propyl-1-benzofuran-6-ol | HCID 15462914 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 3-Phenyl-6-(3-bromopropyloxy)-7-propylbenzofuran | HCID 54011016 | — |
Reaction Steps
To a solution of 3-phenyl-6-hydroxy-7-propylbenzofuran (3.54 g, 13.99 mmol) and potassium carbonate (2.08 g, 15.05 mmol) in dry methyl ethyl ketone (50 ml) was added 1,3-dibromopropane (2.84 ml, 27.98 mmol). The reaction mixture refluxed for 5 hours under nitrogen. The mixture was partitioned between isopropyl acetate and pH4 buffer. The organic was dried over sodium sulfate. The solvent was removed under reduced pressure, and the residue was purified by chromatography (silica gel, 50% methylene chloride in hexane) to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05859051 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-ce050a1f179443c59535ece0b2a55081 |
| Source note | uspto-grants-1999_01 |