HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 68191980, compound → Ethyl 3-(1-(4-fluorophenyl)cyclohexyl)propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 68191980 | HCID 68191980 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ethyl 3-(1-(4-fluorophenyl)cyclohexyl)propanoate | HCID 67168455 | 99.2% |
Reaction Steps
To a solution of (E)-ethyl 3-(1-(4-fluorophenyl)cyclohexyl)acrylate (Intermediate I-7B, 1 g, 3.62 mmol) in methanol (25 mL) was added 10% Pd/C (˜0.5 g, wet 50%) under argon, and the mixture was stirred under hydrogen atmosphere (50 psi) for 16 hrs. The reaction mixture was filtered through CELITE® and evaporated to give the desired ethyl 3-(1-(4-fluorophenyl)cyclohexyl)propanoate (1 g, 99% yield) as an oil. 1H NMR (400 MHz, CDCl3) δ ppm 7.25 (2H, dd, J=9.02, 5.28 Hz), 7.00 (2H, t, J=8.80 Hz), 4.02 (2H, q, J=7.26 Hz), 2.00-2.08 (2H, m), 1.89-1.96 (2H, m), 1.81-1.87 (2H, m), 1.34-1.61 (8H, m), 1.18 (3H, t, J=7.15 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09216972B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-b6ab9930af694c16bd91ebad2fee7015 |
| Source note | uspto-grants-2015_12 |