HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 68430972, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 68430732 | HCID 68430732 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 68430972 | HCID 68430972 | — |
Reaction Steps
To a solution of 5-(4-(2-(3-aminophenyl)ethoxy)phenyl)-3-isoxazolyl pivalate (27.6 mg) in methanol (1 ml), 0.020 ml of acetone, 19.2 mg of sodium cyanoborohydride and 0.05 ml of acetic acid were added, and the reaction solution was stirred at room temperature for 2 hours. The reaction solution was diluted with saturated aqueous hydrogen carbonate sodium, extracted with chloroform, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue obtained was purified by preparative thin layer chromatography (Kieselgel™ 60 F254, Art5744, made by Merck & Co., ethyl acetate/hexane (50:50)) to afford the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367708B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-1db31efa18e9456480933e04a46e8489 |
| Source note | uspto-grants-2013_02 |