HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dibromo-2-(2-bromoethoxy)benzene → 6-Bromo-2,3-dihydro-1-benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dibromo-2-(2-bromoethoxy)benzene | HCID 11473835 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 6-Bromo-2,3-dihydro-1-benzofuran | HCID 11252616 | 98.5% |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
1,4-dibromo-2-(2-bromoethoxy)benzene (136) (922 mg, 2.57 mmol) was dissolved in 25 ml dry THF. After cooled down to −78° C., a solution of 2.5M n-BuLi (1.23 ml, 1.2 q) in hexane was added dropwise. The reaction mixture was stirred at −78° C. for 4 h before poured into ice-water. After extracted twice with ethyl acetate, the org. phase was washed with brine, dried over sodium sulfate and then concentrated to give 504 mg (purity ca 80%) 6-bromo-2,3-dihydrobenzo[b]furan (137) as dark brow oil which was used directly for further reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08546403B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-f76f6ebd679740baa486b91732a5048e |
| Source note | uspto-grants-2013_10 |