HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Octyl-1-benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Nonan-1-oic anhydride | HCID 74304 | — |
| Reactant | (2-Hydroxybenzyl)triphenylphosphonium bromide | HCID 2724142 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Octyl-1-benzofuran | HCID 3787188 | 76.6% |
Reaction Steps
112 g (249 mM) of (2-hydroxybenzyl)triphenylphosphonium bromide, 83 g (278 mM) of nonanoic anhydride, 104 g (1.03 mM) of triethylamine and 800 ml of toluene were placed in a 3 1-three-necked flask, followed by refluxing for 4.5 hours under stirring. After the reaction, the reaction mixture was left standing at room temperature to precipitate a crystal. The crystal was removed by filtration. The filtrate was concentrated and purified by silica gel column chromatography (eluent:toluene/hexane=1/1) to obtain 44 g of liquid 2-octylbenzofuran (Yield: 76.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05733476 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-7cfb9a4aa79d4897a5745b991d796205 |
| Source note | uspto-grants-1998_03 |