HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-(3-Benzoylpropyl)-4-benzamidopiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-4-Piperidylbenzamide | HCID 118120 | — |
| Reactant | 4-Chlorobutyrophenone | HCID 253533 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-(3-Benzoylpropyl)-4-benzamidopiperidine | HCID 10089254 | 9.1% |
Reaction Steps
A mixture of 4-chlorobutyrophenone (447 mg, 2.45 mmol), 4-benzamidopiperidine (500 mg, 2.45 mmol) and K2CO3 (338 mg, 2.45 mmol) was heated up in boiling water bath for 1 hour. The reaction mixture was portioned between water and CHCl3. The organic layer was separated and dried over Na2SO4. After filtration and removal of solvent, the residue was purified by chromatography (SiO2, MeOH:CHCl3, 5:95). Recrystallization from AcOEt/hexane gave a white powder (78 mg, 8.2%). mp 143-144° C.; 1H NMR (CD3OD, 400 MHz) δ1.65 (dq, J1=3.16 Hz, J2=11.9 Hz, 2H), 1.90-2.00 (m, 4H), 2.18 (t, J=11.9 Hz, 2H), 2.48 (m, 2H), 3.00-3.10 (m, 4H), 3.88 (m, 1H), 7.40-8.00 (m, 10H); Mass spectrum (M+1)+ at m/z 351.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06602888B2 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-2c57d1872ace47f39f7aa6e63e33559d |
| Source note | uspto-grants-2003_08 |