HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 2-(Piperidin-1-yl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | o-Fluorobenzaldehyde | HCID 67970 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(Piperidin-1-yl)benzaldehyde | HCID 2062157 | 95.1% |
Reaction Steps
A mixture of o-fluorobenzaldehyde (1.24 gm, 10 mmol), potassium carbonate (2.76 gm, 20 mmol), and piperidine (1.7 gm, 20 mmol) was refluxed in dry DMF for 6 hrs. After the completion of reaction DMF was distilled out at vaccum and 5 ml of water was added to the residue and extracted the product with ethyl acetate (10 ml×2). Organic layer was dried over sodium sulphate and evaporated the solvent to afford 1.8 gm of product (8) (90.5%) 1HNMR CDCl3 (Spectrum 9): 1.68(m, 6H), 3.05(m, 4H), 7.05(m, 2H), 7.45(dd, 1H), 7.75(dd, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07041830B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-528f4103d1a04abd80e280783f2ad730 |
| Source note | uspto-grants-2006_05 |