HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 66839506, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 66839405 | HCID 66839405 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66839506 | HCID 66839506 | 85.8% |
Reaction Steps
TBAF (2.7 mL; 1 M solution in THF) was added to a solution of tert-butyl N′-[5-(tert-butyldiphenylsilanyloxy)-2-(4-fluorophenyl)-3-methylpentanoyl]hydrazinecarboxylate (1.04 g) in THF (20 mL). The reaction solution was stirred at room temperature for 1 hours. Then, ethyl acetate and a saturated ammonium chloride solution were added to the reaction solution, and the organic layer was separated. The resulting organic layer was washed with brine, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (elution solvent: heptane-ethyl acetate system) to obtain 525 mg of the title compound. The property value of the compound is as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07935815B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-626d4923db0842498002bbeaeb9f2108 |
| Source note | uspto-grants-2011_05 |