HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 1,2-Difluoronaphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 1,2,3,4-Tetrafluoronaphthalene | HCID 12343952 | — |
| Reactant | 6-Bromo-1,1,2,2-tetrafluoro-1,2-dihydronaphthalene | HCID 22483437 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,2-Difluoronaphthalene | HCID 11137467 | 95% |
Reaction Steps
A solution of the tetrafluoro naphthalene, 6-bromo-1,1,2,2-tetrafluoro-1,2-dihydronaphthalene (4.74 g, 16.80 mmol) in THF (15 ml) was treated with 30% aqueous NH4OH (30 ml) and zinc (8.45 g, 130 mmol) and stirred under N2 for 24 hours at RT. The reaction was monitored by GC/MS for disappearance of the starting material and found to be complete. The solution was filtered, extracted with hexane (30 ml), and filtered through a short silica column (20 g). The hexane solution was evaporated in vacuo to afford an oil. This crystallized on cooling to room temperature to afford 2.62 g (95% yield) of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06894200B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-3b03b91615c44d2cb19f899240417f06 |
| Source note | uspto-grants-2005_05 |