HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386432Generated: October 30, 2026
Ethanol → Ethyl 3-(4-phenoxyphenyl)propanoate
https://huagongshe.com/reaction/386432
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | ethyl (E)-3-(4-benzylphenyl)acrylate | HCID 67528407 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | Ethyl 3-(4-phenoxyphenyl)propanoate | HCID 20213313 | — |
Reaction Steps
A solution of ethyl (E)-3-(4-benzylphenyl)acrylate (S28, 500 mg, 1.97 mmol) in EtOH (20 mL) was treated with 10% Pd/C (45 mg) and purged with H2. The reaction mixture was stirred overnight at 25° C., filtered through Celite and concentrated to afford S29 (502 mg, 1.96 mmol, 99%) as a yellow oil: 1H NMR (CDCl3, 500 MHz) 7.34 (dd, 2H, J=8.4, 7.4 Hz), 7.17 (d, 2H, J=8.4 Hz), 7.09 (dt, 1H, J=7.7, 1.1 Hz), 7.00 (dd, 2H, J=8.8, 1.1 Hz), 6.95 (d, 2H, J=8.8 Hz), 4.14 (q, 2H, J=7.0 Hz), 2.94 (t, 2H, J=7.7 Hz), 2.63 (t, 2H, J=7.7 Hz), 1.25 (t, 3H, J=7.0 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08372823B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-c214653dd1694eeb9e555beb8f0127f8 |
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| Source note | uspto-grants-2013_02 |
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