HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 86619193, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 3,5-Dichlorobenzaldehyde | HCID 35746 | — |
| Reactant | HCID 86619194 | HCID 86619194 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 86619193 | HCID 86619193 | — |
Reaction Steps
2.22 g (10.1 mmol) of 3-oxo-N-(3-phenylpropyl) butylamide and 1.77 g (10.1 mmol) of 3,5-dichlorobenzaldehyde were dissolved in 30 ml of 2-propanol. 86.0 mg (1.01 mmol) of piperidine and 60.7 mg (1.01 mmol) of acetic acid were added and stirred at room temperature for one day. After the solvent was evaporated under reduced pressure, ethyl acetate was added thereto. The reaction mixture was washed with 1 N hydrochloric acid and then with saturated aqueous sodium hydrogencarbonate solution. The organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by the silica gel chromatography (hexane/ethyl acetate=10/1) to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07288544B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-164cc8f3ef7b4346a781141165556d37 |
| Source note | uspto-grants-2007_10 |