HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 67465999, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 67459904 | HCID 67459904 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67465999 | HCID 67465999 | 99.6% |
Reaction Steps
Lithium borohydride (187 mg) was added to a solution of 5-(3,4,5-trifluorophenyl)piperazine-1,3-dicarboxylic acid 3-ethyl ester 1-methyl ester (991 mg) in THF (20 mL), and the reaction solution was stirred at room temperature for two hours. A saturated ammonium chloride solution and ethyl acetate were added to the reaction solution, and the organic layer was separated. The resulting organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure to obtain 867 mg of a crude product of the title compound. The property value of the compound is as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08048878B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-0e3d713b265b476aa9cad7dbf8d32191 |
| Source note | uspto-grants-2011_11 |