HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → Ethyl 4-(4-benzamidopiperidin-1-yl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl 4-(4-aminopiperidin-1-yl)benzoate | HCID 22557718 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 4-(4-benzamidopiperidin-1-yl)benzoate | HCID 66670912 | 100% |
Reaction Steps
To a solution of ethyl 4-(4-aminopiperidin-1-yl)benzoate (3.0 g, 12.1 mmol) in CH2Cl2 under nitrogen was added Et3N (2.45 g, 24.2 mmol), followed by benzoyl chloride (1.70 g, 12.1 mmol). The mixture was stirred at room temperature overnight, washed with brine (200 mL), dried over anhydrous MgSO4, filtered, and concentrated. The resulting solids were triturated with hexanes to afford ethyl 4-(4-benzamidopiperidin-1-yl)benzoate as a yellow solid (4.2 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238640B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-3dc5a8ba799540dcbebc3efd0229f58f |
| Source note | uspto-grants-2016_01 |