HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → Benzo[b]naphtho[2,1-d]furan
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Reactant | 7,8,9,10-Tetrahydrobenzo[b]naphtho[2,1-d]furan | HCID 268555 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Benzo[b]naphtho[2,1-d]furan | HCID 67460 | 60% |
Reaction Steps
In the atmosphere of argon, 55.5 g of 7,8,9,10-tetrahydrobenzo[b]naphtho[2,1-d]furan, 119 g of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone and 1 L of anhydrous 1,4-dioxane were placed in a flask. The resulting mixture was stirred under reflux for 12 hours. After cooling to room temperature, the reaction solution was extracted with toluene, and deposited solids were filtered out. The filtrate was concentrated by means of a rotary evaporator, and residues were purified by silica gel column chromatography, whereby 32.7 g of (yield: 60%) of benzo[b]naphtho[2,1-d]furan was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08629430B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-873392e5700d4982a706ecc7d3047eff |
| Source note | uspto-grants-2014_01 |