HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847066Generated: October 30, 2026
Sodium Iodide → Ethyl 3-(4-methylphenyl)-3-oxo-2-(allyl)propanoate
https://huagongshe.com/reaction/847066
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Ethyl 3-(4-methylphenyl)-3-oxopropanoate | HCID 292637 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Product | Ethyl 3-(4-methylphenyl)-3-oxo-2-(allyl)propanoate | HCID 15698113 | 97.5% |
Reaction Steps
Ethyl 3-(4-methylphenyl)-3-oxopropanoate (prepared as described in W. Wierenga and H. I. Skulnick, J. Org. Chem. (1979), 44, 310) (63.66 g, 309 mmol, 1 eq) was added to a freshly prepared sodium ethoxide solution (Na, 7.43 g, 323 mmol, 1.05 eq; EtOH, 250 mL). The ethanol was removed in vacuo and the residue was dissolved in DMF (250 mL). Allyl bromide (29.3 mL, 338 mmol, 1.1 eq) followed by sodium iodide (4.56 g, 304 mmol, 1 eq) were then added and the contents stirred overnight at room temperature. The DMF was removed in vacuo, water (250 mL) was added and the aqueous layer extracted with ethyl acetate (3×200 mL). The organic layers were dried (MgSO4) and the solvent removed in vacuo to yield 74.21 g of an amber oil. NMR (200 MHz, CDCl3) δ7.81 (d, 2H, J=10 Hz); 7.30 (d, 2H, J=10 Hz); 5.96-5.72 (m, 1H); 5.21-5.00 (m, 2H); 4.41 (t, 1H, J=7 Hz); 4.16 (q, 2H, J=7 Hz); 2.78 (t, 2H, J=7 Hz); 2.42 (s, 3H); 1.18 (t, 3H, J=7 Hz). Anal. Calcd. for C15H18O3 : C, 73.15; H, 7.37. Found: C, 73.10; H, 7.38.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05138069 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-499effcc12d842abbf7dda768b56687f |
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| Source note | uspto-grants-1992_08 |
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