HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → 2-(Bromomethyl)-1-benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1-Benzofuran-2-Ylmethanol | HCID 2776263 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(Bromomethyl)-1-benzofuran | HCID 12326316 | — |
Reaction Steps
A solution of benzofuran-2-ylmethanol (120 mg; 0.81 mmol) in anh. DCM (5 ml) was treated at rt with CBr4 (268 mg; 0.81 mmol), and with PPh3 (212 mg; 0.81 mmol). The resulting mixture was further stirred at rt, under nitrogen, for 17 h. Concentration to dryness under reduced pressure, and subsequent purification by FC (DCM) afforded 2-(bromomethyl)benzofuran as a yellow oil (128 mg; 75%) which was directly used for the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09242970B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-d9a89dc8e5b345cd95202de71e5886a7 |
| Source note | uspto-grants-2016_01 |