HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 10922777, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 86583681 | HCID 86583681 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 10922777 | HCID 10922777 | 758.3% |
Reaction Steps
A mixture of 2-(phenylcarbonyl)-5-oxohexanoate(3.87 g, 14.8 mmol), acetic acid(130 mg, 2.17 mmol) and piperidine(127 mg, 1.49 mmol) in toluene(5 ml) was refluxed for 5 hr. After cooling down to room temperature, AcOEt was added to the reaction mixture and washed with dil. HCl, water and brine and dried over MgSO4. After removal of the solvent, the residue was purified by column chromatography on silica gel with n-hexane-AcOEt to afford 4.02 g of ethyl 4-oxo-2-phenylcyclohex-2-enecarboxylate(y=94.7%) as a brown oil. 1H-NMR(ppm, 30 MHz, CDCl3) δ 7.50(2H, dd, J=3.0 and 6.4 Hz), 7.40-7.48(3H), 6.47(1H, s), 4.11(2H, q, J=7.0 Hz), 3.96(1H, dd, J=3.7 and 3.7 Hz), 2.60-2.70(1H, m), 2.35-2.55(3H), 1.12(3H, t, J=7.0 Hz)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06271418B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-83beb5b1efae424ba2eba5405e3e6474 |
| Source note | uspto-grants-2001_08 |