HuagongsheHuagongshe Chemistry Print Report · For research reference only
(S)-2-allyloxy-3-(4-benzyloxy-phenyl)-propionic acid ethyl ester → (S)-3-(4-hydroxy-phenyl)-2-propoxy-propionic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (S)-2-allyloxy-3-(4-benzyloxy-phenyl)-propionic acid ethyl ester | HCID 58822773 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (S)-3-(4-hydroxy-phenyl)-2-propoxy-propionic acid ethyl ester | HCID 58822755 | — |
Reaction Steps
A mixture of (S)-2-allyloxy-3-(4-benzyloxy-phenyl)-propionic acid ethyl ester (1.33 mmol, 450 mg) and 10% Pd/C (45 mg) in EtOH (15 mL) were stirred under hydrogen atmosphere (1 atm) for 18 hours. The mixture was filtered through celite and concentrated under vacuum to afford the title product. 1H-NMR (200.15 MHz, CDCl3): δ 7.10 (d, 4H, J=8.6), 6.73 (d, 2H, J=8.4), 5.90 (brs, 1H), 4.16 (q, 2H, J=7.3), 3.94 (t, 1H, J=6.7), 3.53–3.45 (m, 1H), 3.27–3.16 (m, 1H), 2.93 (d, 2H, J=6.5), 1.54 (m, 2H), 1.22 (t, 3H, J=7.3), 0.84 (t, 3H, J=7.5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07192982B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-16f974d918b1437b8bb142662cb3dfa1 |
| Source note | uspto-grants-2007_03 |