HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → Diarachidonyl Methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Diarachidonylmethyl Formate | HCID 58559586 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Diarachidonyl Methanol | HCID 58559615 | 107.4% |
Reaction Steps
The above diarachidonylmethyl formate (III, 0.43 g, 0.71 mmol) and KOH (100 mg) were stirred in 95% EtOH (20 mL) at room temperature under nitrogen overnight. Upon completion of the reaction, most of the solvent was evaporated. The resulting mixture was treated with 20 mL of 2M HCl solution. The aqueous phase was extracted with ether (2×30 mL). The combined ether extract was washed with water (2×25 mL), brine (25 mL), and dried over anhydrous Na2SO4. Evaporation of the solvent gave 0.44 g of IV as pale oil. The crude product was purified by column chromatography on silica gel (230-400 mesh, 40 mL) eluted with 0-5% ethyl acetate gradient in hexanes. This gave 0.41 g of diarachidonyl methanol (IV) as colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09186325B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-93b95b68bbae445288683f043495d90b |
| Source note | uspto-grants-2015_11 |