HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 15487496, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | HCID 22627634 | HCID 22627634 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 15487496 | HCID 15487496 | — |
Reaction Steps
Under nitrogen atmosphere, 0.8 g of 2-cyano-5,6,7,8-tetramethylnaphthalene was dissolved in 30 ml of tetrahydrofuran, and 5.7 ml of a 1.0M solution of diisobutylaluminum hydride in hexane was added to the resulting solution at 0° C. The resulting mixture was stirred at room temperature for 2.5 hours, quenched with methanol and a saturated aqueous solution of ammonium chloride successively, and extracted with ethyl acetate (50 ml×2) . The organic layers were combined, washed with brine, dried over anhydrous magnesium sulfate, and filtered. The resulting filtrate was concentrated and the resulting crude product was purified by silica gel column chromatography to give 0.68 g of the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06121309 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-6ddf6421c638484ba51a2e187992f84b |
| Source note | uspto-grants-2000_09 |