HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 4-(4-oxopiperidin-1-yl)benzoate → Ethyl 4-(4-methylenepiperidin-1-yl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 4-(4-oxopiperidin-1-yl)benzoate | HCID 12717442 | — |
| Reactant | 4-Methylene-1-phenylpiperidine | HCID 58902724 | — |
| Product | Ethyl 4-(4-methylenepiperidin-1-yl)benzoate | HCID 16109082 | — |
Reaction Steps
Using ethyl 4-(4-oxopiperidin-1-yl)benzoate 390B (0.575 g, 2.325 mmol), Wittig olefination was carried out as described for 389A. The title compound was obtained as an off-white crystalline solid (0.338 g, 59.3% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 1.21-1.38 (m, 3H) 2.18-2.30 (m, 4H) 3.37-3.50 (m, 4H) 4.23 (q, J=7.16 Hz, 2H) 4.78 (s, 2H) 6.95-7.04 (m, 2H) 7.72-7.82 (m, 2H). ESI-MS: m/z 246.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08669249B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-de179ae5883e4eb697938a6038e5d41c |
| Source note | uspto-grants-2014_03 |