Sodium Iodide → Ethyl 3-(4-methylphenyl)-3-oxo-2-(allyl)propanoate

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=10Hz); 7.30 (d, 2H, J=10Hz); 5.96-5.72 (m, 1H); 5.21-5.00 (m, 2H); 4.41 (t, 1H, J=7Hz); 4.16 (q, 2H, J=7Hz); 2.78 (t, 2H, J=7Hz); 2.42 (s, 3H); 1.18 (t, 3H, J=7Hz). Anal. Calcd. for C15H18O3 : C, 73.15; H, 7.37. Found: C, 73.10; H, 7.38.

1. customThe ethanol was removed in vacuo
2. dissolutionthe residue was dissolved in DMF (250 mL)
3. additionwere then added
4. customThe DMF was removed in vacuo, water (250 mL)
5. additionwas added
6. extractionthe aqueous layer extracted with ethyl acetate (3×200 mL)
7. dry with materialThe organic layers were dried (MgSO4)
8. customthe solvent removed in vacuo

ORD 기록

ord-e86ceb72609b4b639aeab04fbdd5143f

출처 데이터셋

uspto-grants-1992_07

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US05128355