HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diketene → N-[3-(4,4-Diphenyl-piperidin-1-yl)-propyl]-3-oxo-butyramide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diketene | HCID 12661 | — |
| Reactant | 3-Amino-propyl-4,4-diphenyl piperidine | HCID 10108518 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-[3-(4,4-Diphenyl-piperidin-1-yl)-propyl]-3-oxo-butyramide | HCID 10362296 | 78.2% |
Reaction Steps
Diketene (0.44 mL, 5.68 mmol, 1.3 equiv, Aldrich) was added at room temperature to a stirred solution of 1-(3-aminopropyl) -4-,4-diphenylpiperidine (1.288 g, 4.37 mmol, 1.0 equiv) in anhydrous toluene (15 mL) under argon, and stirring was continued for 48 hours. The mixture was concentrated to give 1.294 g (78%) of white solid, which was used for the next reaction without purification: 1H NMR (300 MHz, CDCl3) δ 1.70 (tt, J=6.4, 6.4 Hz, 2H), 2.23 (s, 3H), 2.44 (br t, J=6.5 Hz), 2.49-2.67 (m, 8H), 3.32 (br t, J=5.8 Hz), 3.36 (s, 2H), 7.16 (m, 2H), 7.27 (m, 8H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05578611 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-d53123b6f2bc461bba2302b60b4132f3 |
| Source note | uspto-grants-1996_11 |